Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Del Rey Tortilleria, Inc. Issues Recall of Flour Tortillas Due to Possible Health Risk
Contact:
Marcy Toledo
773 637-8900
FOR IMMEDIATE RELEASE -- November 12, 2007 -- Del Rey Tortilleria, Inc., Chicago, Illinois, is announcing the recall of its flour tortilla products.
Included in the recall are flour tortillas of all sizes [White Flour Tortillas; Tortillas de Harina(6 inch); Burritos 2, 3, and 4; and Fajita 8" size] with the name "Del Rey" on the label, and with one of these Date Codes: OCT/17/07; OCT/20/07; OCT/24/07; NOV/04/07; NOV/10/07; or NOV/11/07.
Illinois state officials have told us that they believe there is a connection between the tortillas and recent illnesses in Racine, WI schools, in which students experienced vomiting, nausea and abdominal cramps. If you experience symptoms of this type, you should consult a health professional.
State officials have told us that they do not believe the problem involves microbial contamination. Del Rey is not certain that its products caused the reported symptoms, but is recalling the product nevertheless as a precaution while its investigation continues.
This recall does not affect any other Del Rey products.
The products were distributed nationwide through food distributors and grocery stores.
Consumers should immediately return any product that is subject to this recall to the store where it was purchased for a full refund or replacement.
Consumers with questions may contact the company by calling Marcy Toledo, General Manager, at 773 637-8900.
Wednesday, November 14, 2007
Tuesday, November 13, 2007
Napastyle Recalls Romano Pitchers and Tumblers Because of Possible Health Risk
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Napastyle Recalls Romano Pitchers and Tumblers Because of Possible Health Risk
Contact:
Dana Smith
510-524-2066
FOR IMMEDIATE RELEASE -- November 9, 2007 -- NapaStyle of Napa, California is recalling their Romano Pitchers and Tumblers, because they may contain high levels of leachable lead. No illnesses have been reported to date. The recall was a result of an FDA test that showed that the items may contain lead introduced by the manufacturing process by our supplier.
Consumption of leachable lead from the ceramicware can cause severe health problems; especially in infants, young children and pregnant women. High lead exposures can cause a baby to have low birth weight or be born prematurely, or can result in miscarriage or stillbirth. Lead can cause damage to the central nervous system, resulting in learning disabilities and behavioral disorders that could last a lifetime. Children with lead poisoning may not look or act sick.
The Romano Pitchers and Tumblers were distributed through our retail stores in California and nationwide through our mail order catalog.
These pieces are roughly glazed, with streaks of dark brown clay showing through the variegated green finish.
Product Specs:
* Pitcher, 44 oz., 7 1/2" h.
* Four Tumblers, 145 oz., 4 1/4" h
* SKU
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Napastyle Recalls Romano Pitchers and Tumblers Because of Possible Health Risk
Contact:
Dana Smith
510-524-2066
FOR IMMEDIATE RELEASE -- November 9, 2007 -- NapaStyle of Napa, California is recalling their Romano Pitchers and Tumblers, because they may contain high levels of leachable lead. No illnesses have been reported to date. The recall was a result of an FDA test that showed that the items may contain lead introduced by the manufacturing process by our supplier.
Consumption of leachable lead from the ceramicware can cause severe health problems; especially in infants, young children and pregnant women. High lead exposures can cause a baby to have low birth weight or be born prematurely, or can result in miscarriage or stillbirth. Lead can cause damage to the central nervous system, resulting in learning disabilities and behavioral disorders that could last a lifetime. Children with lead poisoning may not look or act sick.
The Romano Pitchers and Tumblers were distributed through our retail stores in California and nationwide through our mail order catalog.
These pieces are roughly glazed, with streaks of dark brown clay showing through the variegated green finish.
Product Specs:
* Pitcher, 44 oz., 7 1/2" h.
* Four Tumblers, 145 oz., 4 1/4" h
* SKU
Friday, November 9, 2007
Kroger Light Caesar Salad Dressing Is Being Recalled
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Kroger Light Caesar Salad Dressing Is Being Recalled
Some bottles are mislabeled and do not list milk, eggs and anchovies as ingredients
Contact:
Meghan Glynn|
(513) 762-1304
FOR IMMEDIATE RELEASE -- Cincinnati, OH -- November 8, 2007 -- The Kroger Co. today announced a recall of Kroger brand 16 oz. Light Caesar Salad Dressing with a Sell By date of May 09 08, a code of SA7221 and a UPC number: 0 11110-71765 8 on the back label.
The salad dressing is being recalled because the back label of the bottle was mislabeled with a Light Asian Salad Dressing label. A small number of cases were released that contain the back label for light Asian Dressing which does not list milk, egg, and anchovies in the ingredient statement or allergen contains statement. People who have an allergy to milk, eggs, and/or anchovies run the risk of serious or life-threatening reaction if they consume this product.
No illnesses have been reported. For most consumers, there is no safety issue with the salad dressing.
The salad dressing may have been distributed to Kroger, Dillons, Food 4 Less (Chicago area only), Jay C, Smith's, Fry's, King Soopers, and City Market grocery stores. No other Kroger-brand salad dressings are affected by this recall.
The mislabeling issue was identified at three Fry's stores in the Phoenix area. The Company is investigating the mislabeling and will enhance labeling procedures to prevent future occurrences.
Customers are encouraged to return the product to the store they purchased it from for a full refund.
Consumers with questions or concerns may call The Kroger Co. at 1-800-632-6900.
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Kroger Light Caesar Salad Dressing Is Being Recalled
Some bottles are mislabeled and do not list milk, eggs and anchovies as ingredients
Contact:
Meghan Glynn|
(513) 762-1304
FOR IMMEDIATE RELEASE -- Cincinnati, OH -- November 8, 2007 -- The Kroger Co. today announced a recall of Kroger brand 16 oz. Light Caesar Salad Dressing with a Sell By date of May 09 08, a code of SA7221 and a UPC number: 0 11110-71765 8 on the back label.
The salad dressing is being recalled because the back label of the bottle was mislabeled with a Light Asian Salad Dressing label. A small number of cases were released that contain the back label for light Asian Dressing which does not list milk, egg, and anchovies in the ingredient statement or allergen contains statement. People who have an allergy to milk, eggs, and/or anchovies run the risk of serious or life-threatening reaction if they consume this product.
No illnesses have been reported. For most consumers, there is no safety issue with the salad dressing.
The salad dressing may have been distributed to Kroger, Dillons, Food 4 Less (Chicago area only), Jay C, Smith's, Fry's, King Soopers, and City Market grocery stores. No other Kroger-brand salad dressings are affected by this recall.
The mislabeling issue was identified at three Fry's stores in the Phoenix area. The Company is investigating the mislabeling and will enhance labeling procedures to prevent future occurrences.
Customers are encouraged to return the product to the store they purchased it from for a full refund.
Consumers with questions or concerns may call The Kroger Co. at 1-800-632-6900.
Wednesday, November 7, 2007
FDA Recall List Change
In order to consistently improve our service to the public, FDA is
implementing a new system for alerting customers when information
important to them has been added or changed on our websites. This free
service is provided by FDA through GovDelivery(r), an email subscription
management service.
Our records show that you have previously subscribed to the FDA Recalls
listserv. To ensure no interruption in this service to you, we will
automatically transfer your subscription to the new system as of
November 15, 2007. You will receive a message confirming your
subscription, from which you may unsubscribe at any time by following
the link to "Subscriber Preferences" in each email alert. FDA e-mail
alerts will come from the address usfda@govdelivery.com.
You may access your Subscriber Preferences to select other FDA topics
that interest you, or sign up to receive additional alerts by entering
your email address wherever you see the "envelope" icon on the FDA
website. You will receive an email message whenever the information you
have chosen is updated on the FDA website.
Your email address will only be used to deliver the information you
request and to give you access to your Subscriber Preferences page,
where you can add or delete subscriptions at any time.
If you have any questions, please send an email to webmail@oc.fda.gov.
Thanks!
FDA Recalls
FDA Recall List Change
implementing a new system for alerting customers when information
important to them has been added or changed on our websites. This free
service is provided by FDA through GovDelivery(r), an email subscription
management service.
Our records show that you have previously subscribed to the FDA Recalls
listserv. To ensure no interruption in this service to you, we will
automatically transfer your subscription to the new system as of
November 15, 2007. You will receive a message confirming your
subscription, from which you may unsubscribe at any time by following
the link to "Subscriber Preferences" in each email alert. FDA e-mail
alerts will come from the address usfda@govdelivery.com.
You may access your Subscriber Preferences to select other FDA topics
that interest you, or sign up to receive additional alerts by entering
your email address wherever you see the "envelope" icon on the FDA
website. You will receive an email message whenever the information you
have chosen is updated on the FDA website.
Your email address will only be used to deliver the information you
request and to give you access to your Subscriber Preferences page,
where you can add or delete subscriptions at any time.
If you have any questions, please send an email to webmail@oc.fda.gov.
Thanks!
FDA Recalls
In order to consistently improve our service to the public, FDA is implementing a new system for alerting customers when information important to them has been added or changed on our websites. This free service is provided by FDA through GovDelivery®, an email subscription management service.
Our records show that you have previously subscribed to the FDA Recalls listserv. To ensure no interruption in this service to you, we will automatically transfer your subscription to the new system as of November 15, 2007. You will receive a message confirming your subscription, from which you may unsubscribe at any time by following the link to &
Tuesday, October 30, 2007
A&M Cookie Company Canada Recalls a Small Number of Presidents Choice Chocolate Chunk Brownie Cookie Packages
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market
withdrawals from the firms involved as a service to consumers, the
media, and other interested parties. FDA does not endorse either the
product or the company. This listserv covers mainly Class I
(life-threatening) recalls. A complete listing of recalls can be found
in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
A&M Cookie Company Canada Recalls a Small Number of Presidents Choice
Chocolate Chunk Brownie Cookie Packages
Contact:
Ray Hehman
415-421-4141
FOR IMMEDIATE RELEASE -- Kitchener, Ontario, Canada -October 25,
2007-A&M Cookie Company Canada is voluntarily recalling the President's
Choice Chocolate Chunk Brownie Cookies, 12 oz, bearing the code date 03
22 08 N, distributed by Sunfresh LLC. The packages subject to recall
contain an undeclared allergen, milk present as a sub ingredient of a
natural flavor. Persons who have an allergy or severe sensitivity to
milk run the risk of possible allergic reactions if they consume these
cookies.
Product Information
Package: President's Choice Chocolate Chunk Brownie Cookies (UPC
041360008305)
Package Code Date: 03 22 08 N
Shipping Case: Shipped in President's Choice Chocolate Chunk Brownie
Cookies (UPC 1 00 41360 00830 2)
Shipping Case Code Date: 03 22 08 N
No other Presidents Choice cookies sold in the USA are affected, and
the Presidents Choice Chocolate Chunk Brownie Cookies sold in Canada
are not affected.
No illnesses or allergenic reactions have been reported. This product
was distributed in Michigan, Iowa, Illinois and Indiana through Jewel
Stores and Wisconsin and Minnesota through Roundy's stores.
The recall was initiated after it was discovered that the milk
containing cookie product was distributed in packaging that did not
reveal the presence of milk. Subsequent investigation indicates that the
problem was caused by mislabeling.
Consumers who have purchased the above President's Choice Chocolate
Chunk Brownie Cookies bearing the code date 03 22 08 N should return the
product back to the store of purchase for a full refund. Media or others
with questions about the recall should contact Ray Hehman of Marketing
Partners Communications, Inc at mkptnr@aol.com or 415 421-4141.
FDA posts press releases and other notices of recalls and market
withdrawals from the firms involved as a service to consumers, the
media, and other interested parties. FDA does not endorse either the
product or the company. This listserv covers mainly Class I
(life-threatening) recalls. A complete listing of recalls can be found
in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
A&M Cookie Company Canada Recalls a Small Number of Presidents Choice
Chocolate Chunk Brownie Cookie Packages
Contact:
Ray Hehman
415-421-4141
FOR IMMEDIATE RELEASE -- Kitchener, Ontario, Canada -October 25,
2007-A&M Cookie Company Canada is voluntarily recalling the President's
Choice Chocolate Chunk Brownie Cookies, 12 oz, bearing the code date 03
22 08 N, distributed by Sunfresh LLC. The packages subject to recall
contain an undeclared allergen, milk present as a sub ingredient of a
natural flavor. Persons who have an allergy or severe sensitivity to
milk run the risk of possible allergic reactions if they consume these
cookies.
Product Information
Package: President's Choice Chocolate Chunk Brownie Cookies (UPC
041360008305)
Package Code Date: 03 22 08 N
Shipping Case: Shipped in President's Choice Chocolate Chunk Brownie
Cookies (UPC 1 00 41360 00830 2)
Shipping Case Code Date: 03 22 08 N
No other Presidents Choice cookies sold in the USA are affected, and
the Presidents Choice Chocolate Chunk Brownie Cookies sold in Canada
are not affected.
No illnesses or allergenic reactions have been reported. This product
was distributed in Michigan, Iowa, Illinois and Indiana through Jewel
Stores and Wisconsin and Minnesota through Roundy's stores.
The recall was initiated after it was discovered that the milk
containing cookie product was distributed in packaging that did not
reveal the presence of milk. Subsequent investigation indicates that the
problem was caused by mislabeling.
Consumers who have purchased the above President's Choice Chocolate
Chunk Brownie Cookies bearing the code date 03 22 08 N should return the
product back to the store of purchase for a full refund. Media or others
with questions about the recall should contact Ray Hehman of Marketing
Partners Communications, Inc at mkptnr@aol.com or 415 421-4141.
Thursday, October 25, 2007
Shain's of Maine Ice Cream Issues Allergy Alert on Undeclared Egg in Kahlua Brownie and Double Fudge Brownie
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Shain's of Maine Ice Cream Issues Allergy Alert on Undeclared Egg in Kahlua Brownie and Double Fudge Brownie
Contact: Jeffrey Shain
207-324-1449
FOR IMMEDIATE RELEASE -- October 17, 2007 -- Shain's of Maine Ice Cream of Sanford, Maine is recalling all quarts of Kahlua Brownie Ice cream, all 3 gallon bulk tubs of Kahlua Brownie Ice cream and all 3 gallon bulk tubs of Double Fudge Brownie Ice cream, because it may contain undeclared egg. People who have an allergy of severe sensitivity to egg run the risk of serious or life threatening allergic reaction if they consume these products.
Kahlua Brownie ice cream and Double Fudge Brownie ice cream was distributed in Maine, New Hampshire, and Massachusetts. It has reached consumers through retail stores, direct delivery and distributors.
Kahlua Brownie ice cream quarts can be identified by the red, black and white labeled cardboard round quart container. This recall affects all lot codes. Kahlua brownie ice cream and double fudge brownie ice cream 3 gallon tubs can be identified by its 3 gallon round bulk cardboard container with the flavor stamped on the top of the container. This recall affects all lots codes.
No illnesses have been reported to date.
The recall was initiated after it was discovered that the brownies in Kahlua Brownie and Double Fudge Brownie were made with a mix that contains egg, that was not declared on the finished product label.
Consumers who have purchased Shain's of Maine Kahlua Brownie or Double Fudge Brownie Ice Cream that are concerned of any egg allergens may return the product to the place of purchase for a full refund. Consumers with any questions may contact Shain's of Maine Ice Cream at 1-800-324-0650.
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Shain's of Maine Ice Cream Issues Allergy Alert on Undeclared Egg in Kahlua Brownie and Double Fudge Brownie
Contact: Jeffrey Shain
207-324-1449
FOR IMMEDIATE RELEASE -- October 17, 2007 -- Shain's of Maine Ice Cream of Sanford, Maine is recalling all quarts of Kahlua Brownie Ice cream, all 3 gallon bulk tubs of Kahlua Brownie Ice cream and all 3 gallon bulk tubs of Double Fudge Brownie Ice cream, because it may contain undeclared egg. People who have an allergy of severe sensitivity to egg run the risk of serious or life threatening allergic reaction if they consume these products.
Kahlua Brownie ice cream and Double Fudge Brownie ice cream was distributed in Maine, New Hampshire, and Massachusetts. It has reached consumers through retail stores, direct delivery and distributors.
Kahlua Brownie ice cream quarts can be identified by the red, black and white labeled cardboard round quart container. This recall affects all lot codes. Kahlua brownie ice cream and double fudge brownie ice cream 3 gallon tubs can be identified by its 3 gallon round bulk cardboard container with the flavor stamped on the top of the container. This recall affects all lots codes.
No illnesses have been reported to date.
The recall was initiated after it was discovered that the brownies in Kahlua Brownie and Double Fudge Brownie were made with a mix that contains egg, that was not declared on the finished product label.
Consumers who have purchased Shain's of Maine Kahlua Brownie or Double Fudge Brownie Ice Cream that are concerned of any egg allergens may return the product to the place of purchase for a full refund. Consumers with any questions may contact Shain's of Maine Ice Cream at 1-800-324-0650.
Lochmead Dairy Issues Allergy Alert on Undeclared Almonds in Lochmead Farms Country Fresh Chocolate Premium Ice Cream
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Lochmead Dairy Issues Allergy Alert on Undeclared Almonds in Lochmead Farms Country Fresh Chocolate Premium Ice Cream
Contact:
Kim Gibson
541-998-8544
FOR IMMEDIATE RELEASE -- Junction City, OR -- October 15, 2007 -- Lochmead Dairy of Junction City, Oregon is recalling half gallons of Lochmead Farms Country Fresh Chocolate Premium Ice Cream with code date June 22, 2008 because they may contain undeclared almonds. People who have allergies or severe sensitivity to almonds run the risk of serious or life-threatening allergic reaction if they consume this product.
The recalled Lochmead Farms Country Fresh Chocolate Premium Ice Cream was distributed by Lochmead Dairy, Inc to Dari Marts and other markets in the Eugene and Corvallis areas.
The product comes in half gallon round containers with "Lochmead Farms Country Fresh Chocolate Premium Ice Cream" on the top label and June 22, 2008 stamped on the bottom.
No illnesses have been reported to date in connection with this problem.
The recall was initiated after it was discovered that the almond-containing product was distributed in packaging that did not reveal the presence of almonds. Subsequent investigation indicates that the problem was caused by a temporary breakdown in the company's production and packaging processes.
Consumers who have purchased Lochmead Farms Country Fresh Chocolate Premium Ice Cream with code date June 22, 2008 are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 541-998-8544.
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Lochmead Dairy Issues Allergy Alert on Undeclared Almonds in Lochmead Farms Country Fresh Chocolate Premium Ice Cream
Contact:
Kim Gibson
541-998-8544
FOR IMMEDIATE RELEASE -- Junction City, OR -- October 15, 2007 -- Lochmead Dairy of Junction City, Oregon is recalling half gallons of Lochmead Farms Country Fresh Chocolate Premium Ice Cream with code date June 22, 2008 because they may contain undeclared almonds. People who have allergies or severe sensitivity to almonds run the risk of serious or life-threatening allergic reaction if they consume this product.
The recalled Lochmead Farms Country Fresh Chocolate Premium Ice Cream was distributed by Lochmead Dairy, Inc to Dari Marts and other markets in the Eugene and Corvallis areas.
The product comes in half gallon round containers with "Lochmead Farms Country Fresh Chocolate Premium Ice Cream" on the top label and June 22, 2008 stamped on the bottom.
No illnesses have been reported to date in connection with this problem.
The recall was initiated after it was discovered that the almond-containing product was distributed in packaging that did not reveal the presence of almonds. Subsequent investigation indicates that the problem was caused by a temporary breakdown in the company's production and packaging processes.
Consumers who have purchased Lochmead Farms Country Fresh Chocolate Premium Ice Cream with code date June 22, 2008 are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 541-998-8544.
Wednesday, October 10, 2007
Wegmans Announces Voluntary Recall of 18 oz. (6-roll pack) Wegmans Food You Feel Good About Country Wheat Rolls
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Wegmans Announces Voluntary Recall of 18 oz. (6-roll pack) Wegmans Food You Feel Good About Country Wheat Rolls
Contact:
Jo Natale
585-429-3627
FOR IMMEDIATE RELEASE -- Rochester, NY -- October 5, 2007 -- Wegmans Food Markets, Inc. is initiating a voluntary recall of 18 oz Wegmans Food You Feel Good About Country Wheat Rolls with best-if-used-by date of October 10. This product is being recalled because the package may actually contain potato rolls, which contain a milk allergen not declared on the label. The bread was produced on Monday, October 1, and would have been available in Wegmans stores between Tuesday, October 2 and Wednesday, October 3. Product with the affected code date is no longer on store shelves.
No illnesses have been reported to date. The recall of this product is of concern only to those individuals who have allergies to milk. Consumption may cause a serious or life-threatening reaction in persons with allergies to milk. Concerned customers should return the product to Wegmans for a full refund. Customers who have consumed the product and feel they are experiencing symptoms should contact their physician.
18 oz Wegmans Food You Feel Good About Country Wheat Rolls are sold exclusively at Wegmans Food Markets located in New York, Pennsylvania, New Jersey, Virginia, and Maryland. Wegmans' customers who have questions or concerns about this recall should contact the consumer affairs department at 1-800-WEGMANS, ext. 4760.
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Wegmans Announces Voluntary Recall of 18 oz. (6-roll pack) Wegmans Food You Feel Good About Country Wheat Rolls
Contact:
Jo Natale
585-429-3627
FOR IMMEDIATE RELEASE -- Rochester, NY -- October 5, 2007 -- Wegmans Food Markets, Inc. is initiating a voluntary recall of 18 oz Wegmans Food You Feel Good About Country Wheat Rolls with best-if-used-by date of October 10. This product is being recalled because the package may actually contain potato rolls, which contain a milk allergen not declared on the label. The bread was produced on Monday, October 1, and would have been available in Wegmans stores between Tuesday, October 2 and Wednesday, October 3. Product with the affected code date is no longer on store shelves.
No illnesses have been reported to date. The recall of this product is of concern only to those individuals who have allergies to milk. Consumption may cause a serious or life-threatening reaction in persons with allergies to milk. Concerned customers should return the product to Wegmans for a full refund. Customers who have consumed the product and feel they are experiencing symptoms should contact their physician.
18 oz Wegmans Food You Feel Good About Country Wheat Rolls are sold exclusively at Wegmans Food Markets located in New York, Pennsylvania, New Jersey, Virginia, and Maryland. Wegmans' customers who have questions or concerns about this recall should contact the consumer affairs department at 1-800-WEGMANS, ext. 4760.
Tuesday, October 9, 2007
Winn-Dixie Stores, Inc. Issues Allergy Alert on Mislabeled Prestige Chocolate Ice Cream
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Winn-Dixie Stores, Inc. Issues Allergy Alert on Mislabeled Prestige Chocolate Ice Cream
Contact:
Winn-Dixie Stores, Inc.
1-866-WINN-DIXIE
FOR IMMEDIATE RELEASE -- Jacksonville, FL -- October 5, 2007 -- Winn-Dixie Stores, Inc. is recalling one code of its 1.75 quart (1.65 liter) cartons of "Prestige Chocolate Ice Cream" because of a potential error in packaging. Some of the products may have the correct lid identifying the product as chocolate almond, but the "tub" is identified as only chocolate. People who have an allergy or severe sensitivity to almonds run the risk of serious or life-threatening allergic reaction if they consume these products. Given this serious issue, the company decided to pull the product from all its stores and encourages customers with any concerns to return the product.
The product comes in an oval 1.75 quart paper carton marked with plant code of 12-356 and an expiration date of JUN 25 08 on a white strip on the side of the carton. The cartons indicate that the product inside is chocolate ice cream while the lid may state that the product is chocolate almond.
The recalled "Prestige Chocolate Ice Cream" was only distributed to Winn-Dixie and Save-Rite stores in Florida, Georgia, Alabama, Louisiana, and Mississippi.
The company has not received any reports from customers in connection with this problem.
The recall was initiated after it was discovered that the almond-containing product was distributed in packaging that did not reveal the presence of almonds.
Subsequent investigation indicates the problem was caused by chocolate ice cream cartons getting on the line while chocolate almond was being produced. The Food and Drug Administration has been informed and there is complete cooperation with them in conducting this recall.
Consumers who have purchased 1.75 quart (1.65 liters) cartons of Prestige Chocolate Ice Cream with JUN 25 08 code date are urged to return them to the place of purchase for a full refund. The cartons indicate that the product inside is chocolate ice cream while the lid may state that the product is chocolate almond.
Consumers with questions or any doubt at all about product in their possession are encouraged to contact the company at 1-866-WINN-DIXIE or return the product to their store for a refund or exchange.
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Winn-Dixie Stores, Inc. Issues Allergy Alert on Mislabeled Prestige Chocolate Ice Cream
Contact:
Winn-Dixie Stores, Inc.
1-866-WINN-DIXIE
FOR IMMEDIATE RELEASE -- Jacksonville, FL -- October 5, 2007 -- Winn-Dixie Stores, Inc. is recalling one code of its 1.75 quart (1.65 liter) cartons of "Prestige Chocolate Ice Cream" because of a potential error in packaging. Some of the products may have the correct lid identifying the product as chocolate almond, but the "tub" is identified as only chocolate. People who have an allergy or severe sensitivity to almonds run the risk of serious or life-threatening allergic reaction if they consume these products. Given this serious issue, the company decided to pull the product from all its stores and encourages customers with any concerns to return the product.
The product comes in an oval 1.75 quart paper carton marked with plant code of 12-356 and an expiration date of JUN 25 08 on a white strip on the side of the carton. The cartons indicate that the product inside is chocolate ice cream while the lid may state that the product is chocolate almond.
The recalled "Prestige Chocolate Ice Cream" was only distributed to Winn-Dixie and Save-Rite stores in Florida, Georgia, Alabama, Louisiana, and Mississippi.
The company has not received any reports from customers in connection with this problem.
The recall was initiated after it was discovered that the almond-containing product was distributed in packaging that did not reveal the presence of almonds.
Subsequent investigation indicates the problem was caused by chocolate ice cream cartons getting on the line while chocolate almond was being produced. The Food and Drug Administration has been informed and there is complete cooperation with them in conducting this recall.
Consumers who have purchased 1.75 quart (1.65 liters) cartons of Prestige Chocolate Ice Cream with JUN 25 08 code date are urged to return them to the place of purchase for a full refund. The cartons indicate that the product inside is chocolate ice cream while the lid may state that the product is chocolate almond.
Consumers with questions or any doubt at all about product in their possession are encouraged to contact the company at 1-866-WINN-DIXIE or return the product to their store for a refund or exchange.
Thursday, October 4, 2007
Kraft Foods Recalls Baker's Premium White Chocolate Baking Squares Because of Possible Health Risk
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Kraft Foods Recalls Baker's Premium White Chocolate Baking Squares Because of Possible Health Risk
Contact:
Cathy Pernu
847-646-3946
FOR IMMEDIATE RELEASE -- Northfield, IL -- October 3, 2007 -- Kraft Foods has issued a recall in the U.S. for Baker's Premium White Chocolate Baking Squares (6 oz.) with a UPC Code 0043000252200 and four best when used by dates:
31 MAR 2008 XCZ
01 APR 2008 XCZ
02 APR 2008 XCZ
03 APR 2008 XCZ
This product may be contaminated with Salmonella, (a bacterium that causes foodborne illness).
Symptoms of foodborne illness caused by Salmonella include fever, diarrhea and abdominal cramps. In persons with poor underlying health or weakened immune systems, Salmonella can invade the bloodstream and cause life-threatening infections.
The product was distributed nationwide. Consumers should not consume the recalled product and should discard any product they may have.
The potential for contamination was noted after testing by the U.S. Food and Drug Administration that detected the presence of Salmonella in some packages of Baker's Premium White Chocolate Baking Squares (6 oz.). The company is aggressively investigating the source of the problem.
This recall is only for Baker's Premium White Chocolate Baking Squares (6 oz.). No other varieties of Baker's White Chocolate or any other Baker's products sold in the United States are impacted by this recall.
Consumers can contact the company at 1-800-310-3704 with any questions they may have or to request reimbursement for purchased product.
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Kraft Foods Recalls Baker's Premium White Chocolate Baking Squares Because of Possible Health Risk
Contact:
Cathy Pernu
847-646-3946
FOR IMMEDIATE RELEASE -- Northfield, IL -- October 3, 2007 -- Kraft Foods has issued a recall in the U.S. for Baker's Premium White Chocolate Baking Squares (6 oz.) with a UPC Code 0043000252200 and four best when used by dates:
31 MAR 2008 XCZ
01 APR 2008 XCZ
02 APR 2008 XCZ
03 APR 2008 XCZ
This product may be contaminated with Salmonella, (a bacterium that causes foodborne illness).
Symptoms of foodborne illness caused by Salmonella include fever, diarrhea and abdominal cramps. In persons with poor underlying health or weakened immune systems, Salmonella can invade the bloodstream and cause life-threatening infections.
The product was distributed nationwide. Consumers should not consume the recalled product and should discard any product they may have.
The potential for contamination was noted after testing by the U.S. Food and Drug Administration that detected the presence of Salmonella in some packages of Baker's Premium White Chocolate Baking Squares (6 oz.). The company is aggressively investigating the source of the problem.
This recall is only for Baker's Premium White Chocolate Baking Squares (6 oz.). No other varieties of Baker's White Chocolate or any other Baker's products sold in the United States are impacted by this recall.
Consumers can contact the company at 1-800-310-3704 with any questions they may have or to request reimbursement for purchased product.
Wednesday, October 3, 2007
Quong Hop & Co. Expands Recall of Tofu
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Quong Hop & Co. Expands Recall of Tofu
Contact:
Quong Hop & Co
650-553-9900
FOR IMMEDIATE RELEASE -- October 1, 2007 -- Quong Hop & Co. of South San Francisco, California is expanding their recall of tofu to include the following products in the following sizes and code dates:
Date Code Product Package Size
1/28/08 or earlier "SOY DELI Five Spice ORGANIC BAKED TOFU" 8 ounce
1/28/08 or earlier "SOY DELI Hickory ORGANIC BAKED TOFU" 8 ounce
1/28/08 or earlier "SOY DELI Honey Sesame ORGANIC BAKED TOFU" 8 ounce
1/28/08 or earlier "SOY DELI Teriyaki ORGANIC BAKED TOFU" 8 ounce
1/28/08 or earlier "SOY DELI Savory ORGANIC BAKED TOFU" 8 ounce
1/28/08 or earlier "SOY DELI Mesquite all natural SMOKED TOFU" 8 ounce
1/28/08 or earlier "SOY DELI Hawaiian Style all natural FRIED TOFU" 8 ounce
1/28/08 or earlier "SOY DELI FIRM ORGANIC NIGARI TOFU" (Vacuum Packed) 8 ounce and 12 ounce
1/28/08 or earlier "SOY DELI All-Natural Tofu Burgers ORIGINAL" 6 ounce
1/28/08 or earlier "SOY DELI All-Natural Tofu Burgers GARDEN" 6 ounce
1/28/08 or earlier "SOY DELI All-Natural Tofu Burgers BARBEQUE" 6 ounce
1/28/08 or earlier "SOY DELI All-Natural Tofu Burgers TERIAKI" 6 ounce
1/28/08 or earlier "SOY DELI All-Natural Tofu Burgers CAJUN" 6 ounce
11/28/07 or earlier "SOY DELI FIRM ORGANIC Gourmet Rich CALCIUM TOFU" (Water Packed, Orange label) 12 ounce
11/28/07 or earlier "SOY DELI SOFT ORGANIC Gourmet Rich CALCIUM TOFU" (Water Packed, Blue label) 12 ounce
11/28/07 or earlier "SOY DELI FIRM ORGANIC NIGARI TOFU" (Water Packed, Red label) 12 ounce
11/28/07 or earlier "QUONG HOP ORGANIC NIGARI TOFU firm style non-pasteurized" (Water Packed, Red label) 16 ounce
11/28/07 or earlier "SOY DELI FIRM ORGANIC NIGARI TOFU" (Vacuum Packed) 30 ounce
11/28/07 or earlier "SOY DELI NIGARI BULK TOFU" 10 pound
11/28/07 or earlier "SOY DELI NIGARI MEDIUM BULK TOFU" 10 pound
11/28/07 or earlier "NIGARI FIRM TOFU 54 PC" (4 oz squares) 10 pound
11/28/07 or earlier "SOY DELI NIGARI FIRM BULK TOFU" 10 pound and 25 pound
11/28/07 or earlier "SOY DELI SOY LOWER CARB RAVIOLI" SOY PASTA 12 ounce
11/28/07 or earlier "SOY DELI SOY LOWER CARB TORTELLINI" SOY PASTA 12 ounce
11/28/07 or earlier "SOY DELI SOY LOWER CARB MANICOTTI" SOY PASTA 12 ounce
These products are being recalled due to finding Listeria monocytogenes in three of our twenty nine products during the Company's sampling and in the three swabs in the manufacturing plant. This extended recall is being done because these items have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Although healthy individuals may suffer only short term symptoms such as high fever, sever headache, stiffness, abdominal pain and diarrhea. Listeria infection in severe cases can cause miscarriages and still births among pregnant women.
The recalled "SOY DELI" and "QUONG HOP" brand products are distributed on the West Coast and Midwest through supermarkets and natural food stores. Product was distributed to the following states: AK, AZ, WA, CA, OR, NV, WI, MO, IL, IN, WY, ND, SD. Due the numbers of states these items are distributed in this is considered a "National Recall" to ensure consumer and trade awareness.
This expanded recall reflects product currently in the market. No additional cases of bacteria have been reported. This is a precaution being taken to help ensure product safety.
The date code can be found on the front panel of all the aforementioned products printed in blue ink.
No illnesses have been reported to date in connection with this problem.
The potential for contamination was noted after a routine test by Washington State Department of Agriculture's Food Safety Program revealed the presence of Listeria monocytogenes in a 12 OZ vacuum pack package of "SOY DELI FIRM ORGANIC NIGARI TOFU". Further testing in two sample lots confirmed that the 12oz , 30 oz and Bulk tofu did contain Listeria monocytogenes. The company working with the State of California is voluntarily recalling all products produced during the same time period as the sampled product to ensure customer safety.
Consumers who have purchased the recalled products are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 650-553-9900 ext 22.
The Company has been in operation for over 100 years and this is our first detection of Listeria. Our primary concern is our consumer's safety.
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Quong Hop & Co. Expands Recall of Tofu
Contact:
Quong Hop & Co
650-553-9900
FOR IMMEDIATE RELEASE -- October 1, 2007 -- Quong Hop & Co. of South San Francisco, California is expanding their recall of tofu to include the following products in the following sizes and code dates:
Date Code Product Package Size
1/28/08 or earlier "SOY DELI Five Spice ORGANIC BAKED TOFU" 8 ounce
1/28/08 or earlier "SOY DELI Hickory ORGANIC BAKED TOFU" 8 ounce
1/28/08 or earlier "SOY DELI Honey Sesame ORGANIC BAKED TOFU" 8 ounce
1/28/08 or earlier "SOY DELI Teriyaki ORGANIC BAKED TOFU" 8 ounce
1/28/08 or earlier "SOY DELI Savory ORGANIC BAKED TOFU" 8 ounce
1/28/08 or earlier "SOY DELI Mesquite all natural SMOKED TOFU" 8 ounce
1/28/08 or earlier "SOY DELI Hawaiian Style all natural FRIED TOFU" 8 ounce
1/28/08 or earlier "SOY DELI FIRM ORGANIC NIGARI TOFU" (Vacuum Packed) 8 ounce and 12 ounce
1/28/08 or earlier "SOY DELI All-Natural Tofu Burgers ORIGINAL" 6 ounce
1/28/08 or earlier "SOY DELI All-Natural Tofu Burgers GARDEN" 6 ounce
1/28/08 or earlier "SOY DELI All-Natural Tofu Burgers BARBEQUE" 6 ounce
1/28/08 or earlier "SOY DELI All-Natural Tofu Burgers TERIAKI" 6 ounce
1/28/08 or earlier "SOY DELI All-Natural Tofu Burgers CAJUN" 6 ounce
11/28/07 or earlier "SOY DELI FIRM ORGANIC Gourmet Rich CALCIUM TOFU" (Water Packed, Orange label) 12 ounce
11/28/07 or earlier "SOY DELI SOFT ORGANIC Gourmet Rich CALCIUM TOFU" (Water Packed, Blue label) 12 ounce
11/28/07 or earlier "SOY DELI FIRM ORGANIC NIGARI TOFU" (Water Packed, Red label) 12 ounce
11/28/07 or earlier "QUONG HOP ORGANIC NIGARI TOFU firm style non-pasteurized" (Water Packed, Red label) 16 ounce
11/28/07 or earlier "SOY DELI FIRM ORGANIC NIGARI TOFU" (Vacuum Packed) 30 ounce
11/28/07 or earlier "SOY DELI NIGARI BULK TOFU" 10 pound
11/28/07 or earlier "SOY DELI NIGARI MEDIUM BULK TOFU" 10 pound
11/28/07 or earlier "NIGARI FIRM TOFU 54 PC" (4 oz squares) 10 pound
11/28/07 or earlier "SOY DELI NIGARI FIRM BULK TOFU" 10 pound and 25 pound
11/28/07 or earlier "SOY DELI SOY LOWER CARB RAVIOLI" SOY PASTA 12 ounce
11/28/07 or earlier "SOY DELI SOY LOWER CARB TORTELLINI" SOY PASTA 12 ounce
11/28/07 or earlier "SOY DELI SOY LOWER CARB MANICOTTI" SOY PASTA 12 ounce
These products are being recalled due to finding Listeria monocytogenes in three of our twenty nine products during the Company's sampling and in the three swabs in the manufacturing plant. This extended recall is being done because these items have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Although healthy individuals may suffer only short term symptoms such as high fever, sever headache, stiffness, abdominal pain and diarrhea. Listeria infection in severe cases can cause miscarriages and still births among pregnant women.
The recalled "SOY DELI" and "QUONG HOP" brand products are distributed on the West Coast and Midwest through supermarkets and natural food stores. Product was distributed to the following states: AK, AZ, WA, CA, OR, NV, WI, MO, IL, IN, WY, ND, SD. Due the numbers of states these items are distributed in this is considered a "National Recall" to ensure consumer and trade awareness.
This expanded recall reflects product currently in the market. No additional cases of bacteria have been reported. This is a precaution being taken to help ensure product safety.
The date code can be found on the front panel of all the aforementioned products printed in blue ink.
No illnesses have been reported to date in connection with this problem.
The potential for contamination was noted after a routine test by Washington State Department of Agriculture's Food Safety Program revealed the presence of Listeria monocytogenes in a 12 OZ vacuum pack package of "SOY DELI FIRM ORGANIC NIGARI TOFU". Further testing in two sample lots confirmed that the 12oz , 30 oz and Bulk tofu did contain Listeria monocytogenes. The company working with the State of California is voluntarily recalling all products produced during the same time period as the sampled product to ensure customer safety.
Consumers who have purchased the recalled products are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 650-553-9900 ext 22.
The Company has been in operation for over 100 years and this is our first detection of Listeria. Our primary concern is our consumer's safety.
Jensen's Old Fashioned Smokehouse Inc. Recalls Jensen's Seattle Style Wild Smoked Salmon Spread Lemon Dill and Onion, Because of Possible Health Risk
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market
withdrawals from the firms involved as a service to consumers, the
media, and other interested parties. FDA does not endorse either the
product or the company. This listserv covers mainly Class I
(life-threatening) recalls. A complete listing of recalls can be found
in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Jensen's Old Fashioned Smokehouse Inc. Recalls Jensen's Seattle Style
Wild Smoked Salmon Spread Lemon Dill and Onion, Because of Possible
Health Risk
Contact:
Jensen's Old Fashioned Smokehouse Inc.
206-364-5569
FOR IMMEDIATE RELEASE -- Seattle, WA -- October 2, 2007 -- Jensen's Old
Fashioned Smokehouse Inc. of Seattle, WA is recalling 936 tubs of
Jensen's Seattle Style Wild Smoked Salmon Spread Lemon Dill and Onion
which was made by Carso's Pasta of Lynnwood, WA because it has the
potential to be contaminated with Listeria monocytogenes, an organism
which can cause serious and sometimes fatal infections in young
children, frail or elderly people, and others with weakened immune
systems. Although healthy individuals may suffer only short-term
symptoms such as high fever, severe headache, stiffness, nausea,
abdominal pain and diarrhea, Listeria infection can cause miscarriages
and stillbirths among pregnant women.
Jensen's Seattle Style Wild Smoked Salmon Spread Lemon Dill and Onion
was distributed in retail stores in Western Washington.
Jensen's Seattle Style Wild Smoked Salmon Spread Lemon Dill and Onion is
coded Sell By 10/20/07. This product was sold in 7 oz. plastic tubs.
No illnesses have been CONFIRMED to date. The recall was the result of
testing by the FDA which revealed that the finished product contained
the bacteria.
Consumers who have purchased Jensen's Seattle Style Wild Smoked Salmon
Spread Lemon Dill and Onion are urged to return it to the place of
purchase for a full refund. Consumers with questions may contact the
Quality Assurance Department at Jensen's Smokehouse at 206-364-5569.
FDA posts press releases and other notices of recalls and market
withdrawals from the firms involved as a service to consumers, the
media, and other interested parties. FDA does not endorse either the
product or the company. This listserv covers mainly Class I
(life-threatening) recalls. A complete listing of recalls can be found
in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Jensen's Old Fashioned Smokehouse Inc. Recalls Jensen's Seattle Style
Wild Smoked Salmon Spread Lemon Dill and Onion, Because of Possible
Health Risk
Contact:
Jensen's Old Fashioned Smokehouse Inc.
206-364-5569
FOR IMMEDIATE RELEASE -- Seattle, WA -- October 2, 2007 -- Jensen's Old
Fashioned Smokehouse Inc. of Seattle, WA is recalling 936 tubs of
Jensen's Seattle Style Wild Smoked Salmon Spread Lemon Dill and Onion
which was made by Carso's Pasta of Lynnwood, WA because it has the
potential to be contaminated with Listeria monocytogenes, an organism
which can cause serious and sometimes fatal infections in young
children, frail or elderly people, and others with weakened immune
systems. Although healthy individuals may suffer only short-term
symptoms such as high fever, severe headache, stiffness, nausea,
abdominal pain and diarrhea, Listeria infection can cause miscarriages
and stillbirths among pregnant women.
Jensen's Seattle Style Wild Smoked Salmon Spread Lemon Dill and Onion
was distributed in retail stores in Western Washington.
Jensen's Seattle Style Wild Smoked Salmon Spread Lemon Dill and Onion is
coded Sell By 10/20/07. This product was sold in 7 oz. plastic tubs.
No illnesses have been CONFIRMED to date. The recall was the result of
testing by the FDA which revealed that the finished product contained
the bacteria.
Consumers who have purchased Jensen's Seattle Style Wild Smoked Salmon
Spread Lemon Dill and Onion are urged to return it to the place of
purchase for a full refund. Consumers with questions may contact the
Quality Assurance Department at Jensen's Smokehouse at 206-364-5569.
Friday, September 28, 2007
Sabanero Inc. Recalls Cheese for Frying and Grating
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Sabanero Inc. Recalls Cheese for Frying and Grating
Contact:
Alfonso Ibañez
305-588-0277
FOR IMMEDIATE RELEASE -- Miami, FL -- September 28, 2007 -- Sabanero Inc. is voluntarily recalling FOR FRYING and GRATING Cheese 5.5 pounds loafs with lot number 177, expiration date of October 22/07 made by COOPERATIVA COLANTA in their San Pedro Plant in Colombia South America. Only products with lot number 177 and expiration date: October 22, 2007 are subject to this recall. Products containing any other dates or references like in 10 oz. or 5.5 Lb. Regular, low Fat or For Frying Cheese are not subject to this recall and should not be returned. This recall was initiated because the Florida Department of Agriculture and Consumer Services revealed a potential for the presence of Staphylococcus aureus.
Please inspect your entire inventory for any of the affected product. If you have any of this recalled date, immediately discontinue use, quarantine the product and return to Sabanero inc. as per the instructions contained in this letter.
This recall is being conducted to the consumer level.
Upon Receipt of this letter, take the following actions:
* This recall extends to the consumer level. Immediately examine your inventory to include this 5.5 Lb. loaf lot
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Sabanero Inc. Recalls Cheese for Frying and Grating
Contact:
Alfonso Ibañez
305-588-0277
FOR IMMEDIATE RELEASE -- Miami, FL -- September 28, 2007 -- Sabanero Inc. is voluntarily recalling FOR FRYING and GRATING Cheese 5.5 pounds loafs with lot number 177, expiration date of October 22/07 made by COOPERATIVA COLANTA in their San Pedro Plant in Colombia South America. Only products with lot number 177 and expiration date: October 22, 2007 are subject to this recall. Products containing any other dates or references like in 10 oz. or 5.5 Lb. Regular, low Fat or For Frying Cheese are not subject to this recall and should not be returned. This recall was initiated because the Florida Department of Agriculture and Consumer Services revealed a potential for the presence of Staphylococcus aureus.
Please inspect your entire inventory for any of the affected product. If you have any of this recalled date, immediately discontinue use, quarantine the product and return to Sabanero inc. as per the instructions contained in this letter.
This recall is being conducted to the consumer level.
Upon Receipt of this letter, take the following actions:
* This recall extends to the consumer level. Immediately examine your inventory to include this 5.5 Lb. loaf lot
Wednesday, September 26, 2007
Quong Hop & Co. Expands Recall of Tofu
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Quong Hop & Co. Expands Recall of Tofu
Contact:
Quong Hop & Co
650-553-9900
FOR IMMEDIATE RELEASE -- September 19, 2007 -- Quong Hop & Co. of South San Francisco, California is expanding their recall of tofu to include the following products in the following sizes and code dates:
* All varieties and sizes of SOY DELI TOFU coded DEC 17 2007
* 30 OZ SOY DELI ORGANIC NIGARI TOFU coded SEP 23 2007 and OCT 17 2007
* 12 OZ SOY DELI TOFU (water packed) coded SEP 23 and OCT 09 2007
* 16 OZ QUONG HOP TOFU (water packed) coded SEP 23 2007
These products are being recalled because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Although healthy individuals may suffer only short term symptoms such as high fever, sever headache, stiffness, abdominal pain and diarrhea, Listeria infection in severe cases can cause miscarriages and still births among pregnant women.
The recalled "SOY DELI" and "QUONG HOP" brand products are distributed in the Midwest and West coast through supermarkets and natural food stores.
This expanded recall reflects product produced during the selected period. No additional cases of bacteria have been reported. This is a precaution being taken to help ensure product safety.
The date code can be found on the front panel of all the aforementioned products printed in blue ink.
No illnesses have been reported to date in connection with this problem.
The potential for contamination was noted after a routine test by Washington State Department of Agriculture's Food Safety Program revealed the presence of Listeria monocytogenes in a 12 OZ vacuum pack package of "SOY DELI FIRM ORGANIC NIGARI TOFU". The company is voluntarily recalling all products produced during the same time period as the sampled product to ensure customer safety.
Consumers who have purchased the recalled products are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 650-553-9900.
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Quong Hop & Co. Expands Recall of Tofu
Contact:
Quong Hop & Co
650-553-9900
FOR IMMEDIATE RELEASE -- September 19, 2007 -- Quong Hop & Co. of South San Francisco, California is expanding their recall
* All varieties and sizes of SOY DELI TOFU coded DEC 17 2007
* 30 OZ SOY DELI ORGANIC NIGARI TOFU coded SEP 23 2007 and OCT 17 2007
* 12 OZ SOY DELI TOFU (water packed) coded SEP 23 and OCT 09 2007
* 16 OZ QUONG HOP TOFU (water packed) coded SEP 23 2007
These products are being recalled because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Although healthy individuals may suffer only short term symptoms such as high fever, sever headache, stiffness, abdominal pain and diarrhea, Listeria infection in severe cases can cause miscarriages and still births among pregnant women.
The recalled "SOY DELI" and "QUONG HOP" brand products are distributed in the Midwest and West coast through supermarkets and natural food stores.
This expanded recall reflects product produced during the selected period. No additional cases of bacteria have been reported. This is a precaution being taken to help ensure product safety.
The date code can be found on the front panel of all the aforementioned products printed in blue ink.
No illnesses have been reported to date in connection with this problem.
The potential for contamination was noted after a routine test by Washington State Department of Agriculture's Food Safety Program revealed the presence of Listeria monocytogenes in a 12 OZ vacuum pack package of "SOY DELI FIRM ORGANIC NIGARI TOFU". The company is voluntarily recalling all products produced during the same time period as the sampled product to ensure customer safety.
Consumers who have purchased the recalled products are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 650-553-9900.
MCP Recalls All "Queso Cincho de Guerrero" Produced by "Quesos Sabrosos Mexicanos" Distributed Between April 16 - June 26 Because of Possible Health Risk
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
MCP Recalls All "Queso Cincho de Guerrero" Produced by "Quesos Sabrosos Mexicanos" Distributed Between April 16 - June 26 Because of Possible Health Risk
Contact:
MCP
630-279-8600
FOR IMMEDIATE RELEASE -- September 18, 2007 -- MCP is recalling the "Queso Cincho de Guerrero" produced by "Quesos Sabrosos Mexicanos" because it has the potential to be contaminated with Salmonella, an organism which can cause serious and serious and sometimes infections in young children, frail or elderly people and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody) nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis, and Staphylococcus aureus which can cause nausea, retching, abdominal pain, diarrhea and prostration.
The recall of Queso Cincho de Guerrero produced by "Quesos Sabrosos" was distributed in Indiana, Michigan, Georgia, Texas, and Illinois in retail stores.
The dry hard Mexican cheese comes in wheels of 35
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
MCP Recalls All "Queso Cincho de Guerrero" Produced by "Quesos Sabrosos Mexicanos" Distributed Between April 16 - June 26 Because of Possible Health Risk
Contact:
MCP
630-279-8600
FOR IMMEDIATE RELEASE -- September 18, 2007 -- MCP is recalling the "Queso Cincho de Guerrero" produced by "Quesos Sabrosos Mexicanos" because it has the potential to be contaminated with Salmonella, an organism which can cause serious and serious and sometimes infections in young children, frail or elderly people and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody) nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis, and Staphylococcus aureus which can cause nausea, retching, abdominal pain, diarrhea and prostration.
The recall of Queso Cincho de Guerrero produced by "Quesos Sabrosos" was distributed in Indiana, Michigan, Georgia, Texas, and Illinois in retail stores.
The dry hard Mexican cheese comes in wheels of 35
Tuesday, September 25, 2007
Department of Consumer Protection Removes Baby's Bliss Gripe Water From Connecticut Stores Following Voluntary Recall
Recall -- State Press Release
This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Department of Consumer Protection Removes Baby's Bliss Gripe Water From Connecticut Stores Following Voluntary Recall
Contact:
Department of Consumer Protection
860-713-6050
FOR IMMEDIATE RELEASE -- HARTFORD, September 24 -- The Department of Consumer Protection has removed a product from three stores where it was sold, following a voluntary recall by the manufacturer and a U.S. Food and Drug Administration (FDA) warning consumers not to drink or serve the beverage.
The product is Baby's Bliss Gripe Water, apple flavor, with a code of 26952V and expiration date of October 2008 (shown as "10/08" on the label), distributed by MOM Enterprises, Inc., of San Rafael, Calif. The FDA confirmed through laboratory analysis the presence of cryptosporidium after investigating the illness of a 6-week-old infant in Minnesota who consumed the product. Cryptosporidium is a parasite that can cause intestinal infections.
"We have identified three stores in the state that have sold this beverage, and we have made sure that the product has been removed from sale," Consumer Protection Commissioner Jerry Farrell, Jr. said. "Consumers who have this item at home should be sure it is not coded and dated as described in the FDA warning. If it is, please do not use the beverage, but discard it immediately."
The three stores known to have carried Baby's Bliss Gripe Water are:
* Over the Moon, Avon
* Bissell Pharmacy, Ridgefield
* Starlight Baby, Southbury
All of the above stores have been contacted by Consumer Protection and are aware of the recall.
The most common symptom of infection is watery diarrhea. Other symptoms can include dehydration, weight loss, stomach cramps or pain, fever, nausea and vomiting. Symptoms generally begin two to ten days after becoming infected with the parasite and generally last one to two weeks. While most people with healthy immune systems will recover without treatment, the infection could be serious or life-threatening for certain individuals. Infants, children and pregnant women are susceptible to dehydration resulting from diarrhea, which can be life-threatening. Individuals with weakened immune systems are also at risk for a more serious and life-threatening form of illness.
Parents of children who have recently consumed apple flavored Baby's Bliss Gripe Water and have these symptoms should seek immediate medical attention. Parents and caregivers who have given this product to their infants and children should be alert for diarrhea and other signs of Cryptosporidium infection.
The product was sold in a four-ounce plastic bottle packaged inside of a cardboard carton, labeled with the following: Baby's Bliss. Pediatrician Recommended Gripe Water. Apple Flavor.
MOM Enterprises, Inc. is fully cooperating with FDA's investigation into the cause of the contamination and is recalling all potentially contaminated products. FDA continues to investigate and will provide updates as more information becomes available. Consumers can call the FDA at 1-888-723-3366.
This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Department of Consumer Protection Removes Baby's Bliss Gripe Water From Connecticut Stores Following Voluntary Recall
Contact:
Department of Consumer Protection
860-713-6050
FOR IMMEDIATE RELEASE -- HARTFORD, September 24 -- The Department of Consumer Protection has removed a product from three stores where it was sold, following a voluntary recall by the manufacturer and a U.S. Food and Drug Administration (FDA) warning consumers not to drink or serve the beverage.
The product is Baby's Bliss Gripe Water, apple flavor, with a code of 26952V and expiration date of October 2008 (shown as "10/08" on the label), distributed by MOM Enterprises, Inc., of San Rafael, Calif. The FDA confirmed through laboratory analysis the presence of cryptosporidium after investigating the illness of a 6-week-old infant in Minnesota who consumed the product. Cryptosporidium is a parasite that can cause intestinal infections.
"We have identified three stores in the state that have sold this beverage, and we have made sure that the product has been removed from sale," Consumer Protection Commissioner Jerry Farrell, Jr. said. "Consumers who have this item at home should be sure it is not coded and dated as described in the FDA warning. If it is, please do not use the beverage, but discard it immediately."
The three stores known to have carried Baby's Bliss Gripe Water are:
* Over the Moon, Avon
* Bissell Pharmacy, Ridgefield
* Starlight Baby, Southbury
All of the above stores have been contacted by Consumer Protection and are aware of the recall.
The most common symptom of infection is watery diarrhea. Other symptoms can include dehydration, weight loss, stomach cramps or pain, fever, nausea and vomiting. Symptoms generally begin two to ten days after becoming infected with the parasite and generally last one to two weeks. While most people with healthy immune systems will recover without treatment, the infection could be serious or life-threatening for certain individuals. Infants, children and pregnant women are susceptible to dehydration resulting from diarrhea, which can be life-threatening. Individuals with weakened immune systems are also at risk for a more serious and life-threatening form of illness.
Parents of children who have recently consumed apple flavored Baby's Bliss Gripe Water and have these symptoms should seek immediate medical attention. Parents and caregivers who have given this product to their infants and children should be alert for diarrhea and other signs of Cryptosporidium infection.
The product was sold in a four-ounce plastic bottle packaged inside of a cardboard carton, labeled with the following: Baby's Bliss. Pediatrician Recommended Gripe Water. Apple Flavor.
MOM Enterprises, Inc. is fully cooperating with FDA's investigation into the cause of the contamination and is recalling all potentially contaminated products. FDA continues to investigate and will provide updates as more information becomes available. Consumers can call the FDA at 1-888-723-3366.
Friday, September 21, 2007
Private Selection=?iso-8859-1?Q?=AE?= Ice Cream Recalled From Ralphs and Fo od 4 Less Stores in California
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Private Selection® Ice Cream Recalled From Ralphs and Food 4 Less Stores in California
Ice Cream May Contain Egg Not Identified On The Label Classic Churned Light Chocolate Chip Cookie Dough Ice Cream Is Only Flavor Involved
Contact:
Meghan Glynn
(513) 762-1304
FOR IMMEDIATE RELEASE -- Cincinnati, OH -- September 20, 2007 -- Inter-American Products, Inc., a division of The Kroger Co. today announced a recall on all codes of Private Selection Classic Churned Light Chocolate Chip Cookie Dough Ice Cream in 1.75-quart containers.
The ice cream is being recalled because it may contain eggs, which are not listed in the ingredient statement. People who have an allergy to eggs run the risk of serious or life-threatening reaction if they consume this product.
The ice cream was distributed only to Ralphs Food Stores in California and Food 4 Less stores in Southern California. No other Private Selection Ice Cream products are affected by this recall.
Customers are encouraged to return the product to a Ralphs or Food 4 Less store for a full refund.
No illnesses have been reported. For most consumers, there is no safety issue with the ice cream. Consumers with questions or concerns may call Inter-American Products, Inc. at 1-800-697-2448.
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Private Selection® Ice Cream Recalled From Ralphs and Food 4 Less Stores in California
Ice Cream May Contain Egg Not Identified On The Label Classic Churned Light Chocolate Chip Cookie Dough Ice Cream Is Only Flavor Involved
Contact:
Meghan Glynn
(513) 762-1304
FOR IMMEDIATE RELEASE -- Cincinnati, OH -- September 20, 2007 -- Inter-American Products, Inc., a division of The Kroger Co. today announced a recall on all codes of Private Selection Classic Churned Light Chocolate Chip Cookie Dough Ice Cream in 1.75-quart containers.
The ice cream is being recalled because it may contain eggs, which are not listed in the ingredient statement. People who have an allergy to eggs run the risk of serious or life-threatening reaction if they consume this product.
The ice cream was distributed only to Ralphs Food Stores in California and Food 4 Less stores in Southern California. No other Private Selection Ice Cream products are affected by this recall.
Customers are encouraged to return the product to a Ralphs or Food 4 Less store for a full refund.
No illnesses have been reported. For most consumers, there is no safety issue with the ice cream. Consumers with questions or concerns may call Inter-American Products, Inc. at 1-800-697-2448.
TWC Global LLC, Inc. Issues a Voluntary Nationwide Recall of Axcil and Desirin Products Marketed as Dietary Supplements
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
TWC Global LLC, Inc. Issues a Voluntary Nationwide Recall of Axcil and Desirin Products Marketed as Dietary Supplements
Contact:
TWC Global, LLC
service@axcil.com
FOR IMMEDIATE RELEASE -- Mountain View, CA -- September 12, 2007 -- TWC Global, LLC, 530 Showers Drive, Suite 7-129, Mountain View, CA 94040, announced today that it is conducting a voluntary nationwide recall of the company's supplement products sold under the names of Axcil and Desirin.
TWC Global is conducting this recall after being informed by representatives of the Food and Drug Administration (FDA) that lab analysis by FDA of Axcil and Desirin samples found the products contain potentially harmful, undeclared ingredients. FDA found the lot of 02B07 contains 3 mg/g of sildenafil, the active ingredient of a FDA-approved drug used for ED, as well as sulfosildenafil and sulfohomosildenafil, both are analogs of sildenafil. All of these undeclared chemicals pose a threat to consumers because they may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may lower blood pressure to dangerous levels.
Consumers with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. Sexual dysfunction is a common problem in men and women with these conditions, and consumers may seek these types of products to enhance sexual performance.
Both Axcil and Desirin are sold on internet nationwide. The products are sold as a 15-capsule blister pack packaged in a box.
Customers who have these products in their possession should stop using them immediately and contact their physician if they have experienced any problems that may be related to taking these products.
Any adverse events that may be related to the use of this product should be reported to the FDA's MedWatch Program by phone at 1-800-FDA-1088 or by fax at 1-800-FDA-0178 or by mail at MedWatch, HF-2, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787.
The company advises that any unused portion of the products be returned to TWC Global, LLC immediately for a full purchase price refund. The returning address is: TWC Global, LLC, 530 Showers Drive, Suite 7-129, Mountain View, CA 94040. Please return the unused portion of the product with invoice for refund. Consumers with questions may contact the company at 650-575-0828.
The Company is taking this voluntary action because it is committed and is always concerned with the health of consumers who have taken these products. The Company is reviewing the raw materials used to make these products and the raw material manufacturers and suppliers to identify the source of contamination to ensure that there will be no future issues with regard to Axcil and Desirin's compositions. The Company is working closely with the FDA in the recall process and is committed to the quality and integrity of its products. It sincerely regrets any inconvenience to consumers.
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
TWC Global LLC, Inc. Issues a Voluntary Nationwide Recall of Axcil and Desirin Products Marketed as Dietary Supplements
Contact:
TWC Global, LLC
service@axcil.com
FOR IMMEDIATE RELEASE -- Mountain View, CA -- September 12, 2007 -- TWC Global, LLC, 530 Showers Drive, Suite 7-129, Mountain View, CA 94040, announced today that it is conducting a voluntary nationwide recall of the company's supplement products sold under the names of Axcil and Desirin.
TWC Global is conducting this recall after being informed by representatives of the Food and Drug Administration (FDA) that lab analysis by FDA of Axcil and Desirin samples found the products contain potentially harmful, undeclared ingredients. FDA found the lot of 02B07 contains 3 mg/g of sildenafil, the active ingredient of a FDA-approved drug used for ED, as well as sulfosildenafil and sulfohomosildenafil, both are analogs of sildenafil. All of these undeclared chemicals pose a threat to consumers because they may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may lower blood pressure to dangerous levels.
Consumers with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. Sexual dysfunction is a common problem in men and women with these conditions, and consumers may seek these types of products to enhance sexual performance.
Both Axcil and Desirin are sold on internet nationwide. The products are sold as a 15-capsule blister pack packaged in a box.
Customers who have these products in their possession should stop using them immediately and contact their physician if they have experienced any problems that may be related to taking these products.
Any adverse events that may be related to the use of this product should be reported to the FDA's MedWatch Program by phone at 1-800-FDA-1088 or by fax at 1-800-FDA-0178 or by mail at MedWatch, HF-2, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787.
The company advises that any unused portion of the products be returned to TWC Global, LLC immediately for a full purchase price refund. The returning address is: TWC Global, LLC, 530 Showers Drive, Suite 7-129, Mountain View, CA 94040. Please return the unused portion of the product with invoice for refund. Consumers with questions may contact the company at 650-575-0828.
The Company is taking this voluntary action because it is committed and is always concerned with the health of consumers who have taken these products. The Company is reviewing the raw materials used to make these products and the raw material manufacturers and suppliers to identify the source of contamination to ensure that there will be no future issues with regard to Axcil and Desirin's compositions. The Company is working closely with the FDA in the recall process and is committed to the quality and integrity of its products. It sincerely regrets any inconvenience to consumers.
Wednesday, September 19, 2007
Quong Hop & Co. Recalls Tofu Because of Possible Health Risk
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market
withdrawals from the firms involved as a service to consumers, the
media, and other interested parties. FDA does not endorse either the
product or the company. This listserv covers mainly Class I
(life-threatening) recalls. A complete listing of recalls can be found
in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Quong Hop & Co. Recalls Tofu Because of Possible Health Risk
Contact:
Quong Hop & Co
650-553-9900
FOR IMMEDIATE RELEASE -- San Francisco, Calif. -- Sept. 19, 2007 ---
Quong Hop & Co. of South San Francisco, California is recalling all SOY
DELI brand tofu with code date DEC 17 2007 and certain varieties of SOY
DELI and QUONG HOP brand tofu with code date SEP 23 2007.
The recall includes the following products in the following sizes and
code dates:
* All varieties and sizes of SOY DELI TOFU coded DEC 17 2007
* 30 OZ SOY DELI NIGARI TOFU coded SEP 23 2007
* 12 OZ SOY DELI WATER PACK TOFU coded SEP 23 2007
* 16 OZ QUONG HOP WATER PACK TOFU coded SEP 23 2007
These products are being recalled because they have the potential to be
contaminated with Listeria monocytogenes, an organism which can cause
serious and sometimes fatal infections in young children, frail or
elderly people and others with weakened immune systems. Although healthy
individuals may suffer only short term symptoms such as high fever,
sever headache, stiffness, abdominal pain and diarrhea, Listeria
infection in severe cases can cause miscarriages and still births among
pregnant women. Consumers experiencing any of these symptoms should seek
immediate medical attention.
The recalled "SOY DELI" and "QUONG HOP" brand products are distributed
in the Midwest and West coast throughout supermarkets and natural food
stores.
The date code can be found on the front panel of all the aforementioned
products printed in blue ink.
No illnesses have been reported to date in connection with this problem.
The potential for contamination was noted after a routine test by
Washington State Department of Agriculture's Food Safety Program
revealed the presence of Listeria monocytogenes in a 12 OZ vacuum pack
package of "SOY DELI FIRM ORGANIC NIGARI TOFU". The company is
voluntarily recalling all products produced during the same time period
as the sampled product to ensure customer safety.
Consumers who have purchased the recalled products are urged to return
them to the place of purchase for a full refund. Consumers with
questions may contact the company at 650-553-9900.
FDA posts press releases and other notices of recalls and market
withdrawals from the firms involved as a service to consumers, the
media, and other interested parties. FDA does not endorse either the
product or the company. This listserv covers mainly Class I
(life-threatening) recalls. A complete listing of recalls can be found
in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Quong Hop & Co. Recalls Tofu Because of Possible Health Risk
Contact:
Quong Hop & Co
650-553-9900
FOR IMMEDIATE RELEASE -- San Francisco, Calif. -- Sept. 19, 2007 ---
Quong Hop & Co. of South San Francisco, California is recalling all SOY
DELI brand tofu with code date DEC 17 2007 and certain varieties of SOY
DELI and QUONG HOP brand tofu with code date SEP 23 2007.
The recall includes the following products in the following sizes and
code dates:
* All varieties and sizes of SOY DELI TOFU coded DEC 17 2007
* 30 OZ SOY DELI NIGARI TOFU coded SEP 23 2007
* 12 OZ SOY DELI WATER PACK TOFU coded SEP 23 2007
* 16 OZ QUONG HOP WATER PACK TOFU coded SEP 23 2007
These products are being recalled because they have the potential to be
contaminated with Listeria monocytogenes, an organism which can cause
serious and sometimes fatal infections in young children, frail or
elderly people and others with weakened immune systems. Although healthy
individuals may suffer only short term symptoms such as high fever,
sever headache, stiffness, abdominal pain and diarrhea, Listeria
infection in severe cases can cause miscarriages and still births among
pregnant women. Consumers experiencing any of these symptoms should seek
immediate medical attention.
The recalled "SOY DELI" and "QUONG HOP" brand products are distributed
in the Midwest and West coast throughout supermarkets and natural food
stores.
The date code can be found on the front panel of all the aforementioned
products printed in blue ink.
No illnesses have been reported to date in connection with this problem.
The potential for contamination was noted after a routine test by
Washington State Department of Agriculture's Food Safety Program
revealed the presence of Listeria monocytogenes in a 12 OZ vacuum pack
package of "SOY DELI FIRM ORGANIC NIGARI TOFU". The company is
voluntarily recalling all products produced during the same time period
as the sampled product to ensure customer safety.
Consumers who have purchased the recalled products are urged to return
them to the place of purchase for a full refund. Consumers with
questions may contact the company at 650-553-9900.
Bravo! Issues Nationwide Recall of Select Poultry Products for Dogs and Cats
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market
withdrawals from the firms involved as a service to consumers, the
media, and other interested parties. FDA does not endorse either the
product or the company. This listserv covers mainly Class I
(life-threatening) recalls. A complete listing of recalls can be found
in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Bravo! Issues Nationwide Recall of Select Poultry Products for Dogs and
Cats
Contact:
David Bogner
(866) 922-9222
FOR IMMEDIATE RELEASE --Vernon, CT -- Sept. 18, 2007--- Bravo! announces
a voluntary recall of select tubes of three of its poultry products for
cats and dogs. The pet food is being recalled because two of the
products have the potential to be contaminated with Salmonella and
Listeria monocytogenes, while the other product has the potential to be
contaminated with Listeria monocytogenes.
Both Salmonella and Listeria are organisms which can cause serious
infections in dogs and cats, and if there is cross contamination, in
people, especially small children, frail or elderly people, and others
with weakened immune systems. Healthy people with Salmonella infection
may only suffer short-term symptoms, such as high fever, severe
headache, vomiting, nausea, abdominal pain, and diarrhea. Long term
complications can include arthritis and other more serious ailments.
Healthy people with Listeria infection may only suffer short-term
symptoms such as high fever, severe headache, stiffness, nausea,
abdominal pain, and diarrhea. Listeria infection can cause miscarriages
and stillbirths among pregnant women.
The company has received no reports of illness in either people or
animals associated with any of the three products.
The recalled products are distributed nationwide to distributors, retail
stores, internet sales and directly to consumers, and they can be
identified by the batch ID code located on the hang tag attached to the
bottom of the plastic film tubes. The recalled products should not be
sold or fed to pets. Pet owners should return unopened frozen tubes of
food to the store where purchased for a full refund. Pet owners should
dispose of opened tubes of product in a safe manner (example, a securely
covered trash receptacle) and return the washed plastic batch ID tag to
the store where purchased for a full refund.
Recalled Pet Food
Product: Bravo Original Formula Chicken Blend frozen raw food
Product Numbers: 21-102, 21-105, 21-110
Sizes: 2 pound, 5 pound and 10 pound tubes
Batch ID code (on hang tag): 236
Reason for Recall: Salmonella, Listeria
Product: Bravo Original Formula Turkey Blend frozen raw food
Product Numbers: 31-102, 31-105, 31-110
Sizes: 2 pound, 5 pound and 10 pound tubes
Batch ID code (on hang tag): 236
Reason for Recall: Listeria
Product: Bravo Basic Formula Finely Ground Chicken frozen raw food
Product Number: 21-212
Size: 2 pound tube
Batch ID Code (on hang tag): 226
Reason for Recall: Salmonella, Listeria
Other Batch IDs for these same products are not involved in the recall.
Bravo! is issuing this action out of an abundance of caution and
sincerely regrets any inconvenience to pet owners as a result of this
announcement. This voluntary recall has been issued because the FDA
detected the bacteria in samples during a recent review.
In an effort to prevent the transmission of Salmonella from pets to
family members and care givers, the FDA recommends that everyone follow
appropriate pet food handling guidelines when feeding their pets. A
list of safe pet food handling tips can be found at:
http://www.fda.gov/cvm/CVM_Updates/foodbornetips.htm.
People may risk Salmonella infection not only by handling these pet
foods, but also by contact with pets or other surfaces exposed to these
foods, so it is important that they thoroughly wash their hands with hot
water and soap. Anyone who is experiencing the symptoms of Salmonella
or Listeria infection after having handled the recalled product should
seek medical attention. Consumers may report any complaints to FDA's
local District Complaint Coordinator's located on the FDA website:
http://www.fda.gov/opacom/backgrounders/complain.html.
Healthy cats and dogs rarely become sick from Salmonella. Animals ill
with Salmonella will display symptoms similar to the ones listed above
for humans. People who have concerns about whether their pet has
Salmonella or not should contact their veterinarian.
For more information on the Bravo recall, please visit
www.bravorawdiet.com , or call toll free
(866) 922-9222
FDA posts press releases and other notices of recalls and market
withdrawals from the firms involved as a service to consumers, the
media, and other interested parties. FDA does not endorse either the
product or the company. This listserv covers mainly Class I
(life-threatening) recalls. A complete listing of recalls can be found
in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Bravo! Issues Nationwide Recall of Select Poultry Products for Dogs and
Cats
Contact:
David Bogner
(866) 922-9222
FOR IMMEDIATE RELEASE --Vernon, CT -- Sept. 18, 2007--- Bravo! announces
a voluntary recall of select tubes of three of its poultry products for
cats and dogs. The pet food is being recalled because two of the
products have the potential to be contaminated with Salmonella and
Listeria monocytogenes, while the other product has the potential to be
contaminated with Listeria monocytogenes.
Both Salmonella and Listeria are organisms which can cause serious
infections in dogs and cats, and if there is cross contamination, in
people, especially small children, frail or elderly people, and others
with weakened immune systems. Healthy people with Salmonella infection
may only suffer short-term symptoms, such as high fever, severe
headache, vomiting, nausea, abdominal pain, and diarrhea. Long term
complications can include arthritis and other more serious ailments.
Healthy people with Listeria infection may only suffer short-term
symptoms such as high fever, severe headache, stiffness, nausea,
abdominal pain, and diarrhea. Listeria infection can cause miscarriages
and stillbirths among pregnant women.
The company has received no reports of illness in either people or
animals associated with any of the three products.
The recalled products are distributed nationwide to distributors, retail
stores, internet sales and directly to consumers, and they can be
identified by the batch ID code located on the hang tag attached to the
bottom of the plastic film tubes. The recalled products should not be
sold or fed to pets. Pet owners should return unopened frozen tubes of
food to the store where purchased for a full refund. Pet owners should
dispose of opened tubes of product in a safe manner (example, a securely
covered trash receptacle) and return the washed plastic batch ID tag to
the store where purchased for a full refund.
Recalled Pet Food
Product: Bravo Original Formula Chicken Blend frozen raw food
Product Numbers: 21-102, 21-105, 21-110
Sizes: 2 pound, 5 pound and 10 pound tubes
Batch ID code (on hang tag): 236
Reason for Recall: Salmonella, Listeria
Product: Bravo Original Formula Turkey Blend frozen raw food
Product Numbers: 31-102, 31-105, 31-110
Sizes: 2 pound, 5 pound and 10 pound tubes
Batch ID code (on hang tag): 236
Reason for Recall: Listeria
Product: Bravo Basic Formula Finely Ground Chicken frozen raw food
Product Number: 21-212
Size: 2 pound tube
Batch ID Code (on hang tag): 226
Reason for Recall: Salmonella, Listeria
Other Batch IDs for these same products are not involved in the recall.
Bravo! is issuing this action out of an abundance of caution and
sincerely regrets any inconvenience to pet owners as a result of this
announcement. This voluntary recall has been issued because the FDA
detected the bacteria in samples during a recent review.
In an effort to prevent the transmission of Salmonella from pets to
family members and care givers, the FDA recommends that everyone follow
appropriate pet food handling guidelines when feeding their pets. A
list of safe pet food handling tips can be found at:
http://www.fda.gov/cvm/CVM_Updates/foodbornetips.htm.
People may risk Salmonella infection not only by handling these pet
foods, but also by contact with pets or other surfaces exposed to these
foods, so it is important that they thoroughly wash their hands with hot
water and soap. Anyone who is experiencing the symptoms of Salmonella
or Listeria infection after having handled the recalled product should
seek medical attention. Consumers may report any complaints to FDA's
local District Complaint Coordinator's located on the FDA website:
http://www.fda.gov/opacom/backgrounders/complain.html.
Healthy cats and dogs rarely become sick from Salmonella. Animals ill
with Salmonella will display symptoms similar to the ones listed above
for humans. People who have concerns about whether their pet has
Salmonella or not should contact their veterinarian.
For more information on the Bravo recall, please visit
www.bravorawdiet.com
(866) 922-9222
Tuesday, September 18, 2007
Dole Fresh Vegetables Announces Voluntary Recall of 'Dole Hearts Delight' Packaged Salads
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market
withdrawals from the firms involved as a service to consumers, the
media, and other interested parties. FDA does not endorse either the
product or the company. This listserv covers mainly Class I
(life-threatening) recalls. A complete listing of recalls can be found
in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Dole Fresh Vegetables Announces Voluntary Recall of 'Dole Hearts
Delight' Packaged Salads
Contact:
Marty Ordman
1-818-874-4834
FOR IMMEDIATE RELEASE --Monterey, Calif. -- Sept. 17, 2007 --- Dole
Fresh Vegetables, a division of Dole Food Company, Inc., today announced
that it is voluntarily recalling all salad bearing the label "Dole
Hearts Delight" sold in the U.S. and Canada with a "best if used by
(BIUB)" date of September 19, 2007, and a production code of "A24924A"
or "A24924B" stamped on the package. The "best if use by (BIUB)" code
date can be located in the upper right hand corner of the front of the
bag. The salad was sold in plastic bags of 227 grams in Canada and
one-half pound in the U.S., with UPC code 071430-01038.
Symptoms of E. coli O157:H7 exposure could include stomach cramps and
diarrhea. Bloody diarrhea may develop. E. coli disease sometimes leads
to a complication called hemolytic uremic syndrome (HUS). If you
exhibited any of these symptoms within 3 to 5 days of consuming any of
the products specified above, seek medical attention.
To date, Dole has received no reports that anyone has become sick from
eating these products. The recall is occurring because a sample in a
grocery store in Canada was found through random screening to contain E.
coli O157:H7. No other Dole salad products are involved.
Eric Schwartz, President, Dole Fresh Vegetables, stated: "Our
overriding concern is for consumer safety. We are working closely with
the U.S. Food and Drug Administration, the Canadian Food Inspection
Agency, and several U.S. state health departments."
Consumers who may still have any of the "Dole Hearts Delight" salads
with a "best if used by date" of September 19 and a production code of
"A24924A" or "A24924B" should dispose of the product. This product was
sold in Ontario, Quebec and the Maritime Provinces in Canada and in
Illinois, Indiana, Maine, Michigan, Mississippi, New York, Ohio,
Pennsylvania, Tennessee and neighboring states in the U.S. Consumers
can call the Dole Consumer Center toll-free at 800-356-3111. Consumers
are reminded that products should not be consumed after the "best if
used by" date.
Dole Food Company, Inc., with 2006 revenues of $6.2 billion, is the
world's largest producer and marketer of high-quality fresh fruit, fresh
vegetables and fresh-cut flowers. Dole markets a growing line of
packaged and frozen foods and is a produce industry leader in nutrition
education and research.
This release contains "forward-looking statements," within the meaning
of the Private Securities Litigation Reform Act of 1995 that involve a
number of risks and uncertainties. Forward looking statements, which are
based on management's current expectations, are generally identifiable
by the use of terms such as "may," "will," "expects," "believes,"
"intends" and similar expressions. The potential risks and uncertainties
that could cause actual results to differ materially from those
expressed or implied herein include weather-related phenomena; market
responses to industry volume pressures; product and raw materials
supplies and pricing; changes in interest and currency exchange rates;
economic crises and security risks in developing countries;
international conflict; and quotas, tariffs and other governmental
actions. Further information on the factors that could affect Dole's
financial results is included in its SEC filings, including its Annual
Report on Form 10-K.
FDA posts press releases and other notices of recalls and market
withdrawals from the firms involved as a service to consumers, the
media, and other interested parties. FDA does not endorse either the
product or the company. This listserv covers mainly Class I
(life-threatening) recalls. A complete listing of recalls can be found
in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Dole Fresh Vegetables Announces Voluntary Recall of 'Dole Hearts
Delight' Packaged Salads
Contact:
Marty Ordman
1-818-874-4834
FOR IMMEDIATE RELEASE --Monterey, Calif. -- Sept. 17, 2007 --- Dole
Fresh Vegetables, a division of Dole Food Company, Inc., today announced
that it is voluntarily recalling all salad bearing the label "Dole
Hearts Delight" sold in the U.S. and Canada with a "best if used by
(BIUB)" date of September 19, 2007, and a production code of "A24924A"
or "A24924B" stamped on the package. The "best if use by (BIUB)" code
date can be located in the upper right hand corner of the front of the
bag. The salad was sold in plastic bags of 227 grams in Canada and
one-half pound in the U.S., with UPC code 071430-01038.
Symptoms of E. coli O157:H7 exposure could include stomach cramps and
diarrhea. Bloody diarrhea may develop. E. coli disease sometimes leads
to a complication called hemolytic uremic syndrome (HUS). If you
exhibited any of these symptoms within 3 to 5 days of consuming any of
the products specified above, seek medical attention.
To date, Dole has received no reports that anyone has become sick from
eating these products. The recall is occurring because a sample in a
grocery store in Canada was found through random screening to contain E.
coli O157:H7. No other Dole salad products are involved.
Eric Schwartz, President, Dole Fresh Vegetables, stated: "Our
overriding concern is for consumer safety. We are working closely with
the U.S. Food and Drug Administration, the Canadian Food Inspection
Agency, and several U.S. state health departments."
Consumers who may still have any of the "Dole Hearts Delight" salads
with a "best if used by date" of September 19 and a production code of
"A24924A" or "A24924B" should dispose of the product. This product was
sold in Ontario, Quebec and the Maritime Provinces in Canada and in
Illinois, Indiana, Maine, Michigan, Mississippi, New York, Ohio,
Pennsylvania, Tennessee and neighboring states in the U.S. Consumers
can call the Dole Consumer Center toll-free at 800-356-3111. Consumers
are reminded that products should not be consumed after the "best if
used by" date.
Dole Food Company, Inc., with 2006 revenues of $6.2 billion, is the
world's largest producer and marketer of high-quality fresh fruit, fresh
vegetables and fresh-cut flowers. Dole markets a growing line of
packaged and frozen foods and is a produce industry leader in nutrition
education and research.
This release contains "forward-looking statements," within the meaning
of the Private Securities Litigation Reform Act of 1995 that involve a
number of risks and uncertainties. Forward looking statements, which are
based on management's current expectations, are generally identifiable
by the use of terms such as "may," "will," "expects," "believes,"
"intends" and similar expressions. The potential risks and uncertainties
that could cause actual results to differ materially from those
expressed or implied herein include weather-related phenomena; market
responses to industry volume pressures; product and raw materials
supplies and pricing; changes in interest and currency exchange rates;
economic crises and security risks in developing countries;
international conflict; and quotas, tariffs and other governmental
actions. Further information on the factors that could affect Dole's
financial results is included in its SEC filings, including its Annual
Report on Form 10-K.
Friday, September 14, 2007
B. Braun Medical Inc. Issues Nationwide Recall of Normal Saline Flush Syringes with Lot Numbers Ending in "SFR"
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
B. Braun Medical Inc. Issues Nationwide Recall of Normal Saline Flush Syringes with Lot Numbers Ending in "SFR"
Contact:
B. Braun Medical Inc.
(800) 227-2862
FOR IMMEDIATE RELEASE -- September 14, 2007 - B. Braun Medical Inc., Bethlehem, PA, announced on July 30, 2007 a voluntary nationwide recall of Normal Saline Flush syringes with lot numbers ending in "SFR" due to an increase in customer complaints for particulate matter in the saline. The FDA has been apprised of this action.
The introduction of particulate matter into the blood stream may result in phlebitis and / or damage to vital organs such as the brain, kidneys, heart and lungs. To a less likely extent, there is a potential for the development of pulmonary embolism or silicone embolism syndrome, which could cause severe injury and / or death. Symptoms would generally be expected to develop quickly and are unlikely to develop more than 24 - 48 hours after the administration of the product. However, the risk associated with use of this product is cumulative and increases with each additional exposure. A patient may not develop any symptoms until they have received multiple doses of the product. To date, B. Braun has received no reports of any patient injury associated with this issue.
Customers that have the recalled product in their possession should discontinue use immediately and contact their physician if they have experienced any problems that may be related to usage of this product. Customers that have the affected product in their possession may contact the B. Braun Medical Inc. Customer Support Department at (800) 227-2862, Monday through Friday, 8 AM to 7 PM EST for instructions for handling the affected product and to arrange for replacement product.
This voluntary recall affects normal saline 3mL in 12mL syringes, designated by product code 513584, and normal saline 10mL in 12mL syringes, designated by product code 513587. Between June 11 and July 18 of this year, B. Braun Medical Inc. distributed approximately 33,000 units of product code 513584 and 1.2 million units of product code 513587 of lot numbers ending in "SFR" to hospitals and distributors. The product code, identified as REF, and lot number, identified as LOT, can be found on the syringe label just below the product description.
These flush syringes have been found to contain particulate matter, which has been identified as a medical grade silicone. While this silicone is biocompatible, routinely used in the medical device industry and is an expected component of these syringes, the visible particulate matter caused by the silicone in these "SFR" lots may pose a health risk.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
* Online: www.fda.gov/medwatch/report.htm
* Regular Mail: use postage-paid FDA form 3500 available at:
www.fda.gov/MedWatch/getforms.htm.
Mail to MedWatch 5600 Fishers Lane, Rockville, MD
20852-9787
* Fax: 1-800-FDA-0178
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
B. Braun Medical Inc. Issues Nationwide Recall of Normal Saline Flush Syringes with Lot Numbers Ending in "SFR"
Contact:
B. Braun Medical Inc.
(800) 227-2862
FOR IMMEDIATE RELEASE -- September 14, 2007 - B. Braun Medical Inc., Bethlehem, PA, announced on July 30, 2007 a voluntary nationwide recall of Normal Saline Flush syringes with lot numbers ending in "SFR" due to an increase in customer complaints for particulate matter in the saline. The FDA has been apprised of this action.
The introduction of particulate matter into the blood stream may result in phlebitis and / or damage to vital organs such as the brain, kidneys, heart and lungs. To a less likely extent, there is a potential for the development of pulmonary embolism or silicone embolism syndrome, which could cause severe injury and / or death. Symptoms would generally be expected to develop quickly and are unlikely to develop more than 24 - 48 hours after the administration of the product. However, the risk associated with use of this product is cumulative and increases with each additional exposure. A patient may not develop any symptoms until they have received multiple doses of the product. To date, B. Braun has received no reports of any patient injury associated with this issue.
Customers that have the recalled product in their possession should discontinue use immediately and contact their physician if they have experienced any problems that may be related to usage of this product. Customers that have the affected product in their possession may contact the B. Braun Medical Inc. Customer Support Department at (800) 227-2862, Monday through Friday, 8 AM to 7 PM EST for instructions for handling the affected product and to arrange for replacement product.
This voluntary recall affects normal saline 3mL in 12mL syringes, designated by product code 513584, and normal saline 10mL in 12mL syringes, designated by product code 513587. Between June 11 and July 18 of this year, B. Braun Medical Inc. distributed approximately 33,000 units of product code 513584 and 1.2 million units of product code 513587 of lot numbers ending in "SFR" to hospitals and distributors. The product code, identified as REF, and lot number, identified as LOT, can be found on the syringe label just below the product description.
These flush syringes have been found to contain particulate matter, which has been identified as a medical grade silicone. While this silicone is biocompatible, routinely used in the medical device industry and is an expected component of these syringes, the visible particulate matter caused by the silicone in these "SFR" lots may pose a health risk.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
* Online: www.fda.gov/medwatch/report.htm
* Regular Mail: use postage-paid FDA form 3500 available at:
www.fda.gov/MedWatch/getforms.htm.
Mail to MedWatch 5600 Fishers Lane, Rockville, MD
20852-9787
* Fax: 1-800-FDA-0178
Tuesday, September 11, 2007
Strong America Limited Issues Alert on Undeclared Sulfites in Great Wall Brand Chinese Wolfberry
Strong America Limited Issues Alert on Undeclared Sulfites in Great Wall
Brand Chinese Wolfberry
Contact:
Mr. Yang
(718) 628-6200
FOR IMMEDIATE RELEASE -- Long Island City, NY -- September 10, 2007 --
Strong America Ltd. of Long Island City, NY is recalling Chinese
Wolfberry, because it may contain undeclared sulfites. People who have a
severe sensitivity to sulfites run the risk of serious or
life-threatening reactions if they consume this product.
The recalled Great Wall brand Chinese Wolfberry is packed in uncoded 7oz
packages and were sold in GA, NY, and TN.
No illnesses have been reported to date.
The recall was initiated after routine sampling by the New York State
Department of Agriculture and Markets Food Inspectors and subsequent
analysis by the Department's Food Laboratory personnel revealed the
presence of sulfites in the product, which were not declared on the
label. The consumption of 10 milligrams of sulfites per serving has been
reported to elicit severe reactions in some asthmatics; Anaphylactic
shock could occur in certain sulfites sensitive individuals upon
ingesting 10 milligrams or more of sulfites. Analysis of the Chinese
Wolfberry revealed that it contained 12.87 milligrams per serving.
Consumers who have Great Wall brand Chinese Wolfberry can return the
product to the place of purchase for a full refund. Consumers with
questions may contact the company at 718-628-6200
Monday, September 10, 2007
Abbott Notifies Users of Precision XtraT, OptiumT, ReliOnR Ultima, Rite AidR and KrogerR Blood Glucose Meters to Check Display Screens
Urgent: Abbott Notifies Users of Precision Xtra(tm), Optium(tm),
ReliOn(r) Ultima, Rite Aid(r) and Kroger(r) Blood Glucose Meters to
Check Display Screens
Contact:
Tama Antonia Donaldson
(510) 749-5449
FOR IMMEDIATE RELEASE -- Alameda, CA -- August 31, 2007 -- Abbott is
initiating a worldwide medical device correction for users of its
Precision Xtra(tm), Optium(tm), ReliOn(r) Ultima, Rite Aid(r) and
Kroger(r) blood glucose meters manufactured after January 31, 2007. If
the meter is dropped on a hard surface, part or all of the display
screen may not work properly or may appear blank, which could result in
an inability to view blood glucose test results. The inability to
generate blood glucose results could result in significant risk for
hypoglycemia or hyperglycemia.
Users of these meters who note that the display screen is not working
properly should immediately stop using their meter as referenced in the
User Guide and call Abbott Diabetes Care customer care for assistance at
1-877-844-4404. Through internal testing, Abbott Diabetes Care has found
that when recently produced meters are dropped onto a hard surface, part
of the display can be jarred or disconnected, thereby making it
difficult to read the lot number or date information, or causing the
screen to appear blank. No injuries have been reported to date.
Patients should keep their glucose meters in the wallet provided to
offer additional protection for the meter. If the meter is dropped on a
hard surface, patients should immediately perform a meter display check.
Instructions on how to do this are detailed in the meter's Users Guide.
If no problems are encountered during the automatic display check, the
meter is ready for use. Customers may call Abbott Diabetes Care customer
care at 1-877-844-4404 to determine the date their meter was
manufactured. Customers may also call customer care if they have
questions or need a replacement meter.
Precision Xtra(tm), Optium, ReliOn(r) Ultima, Rite Aid(r) and Kroger(r)
blood glucose meters have been distributed via retail and mail order
pharmacies, physician offices and distributors. Abbott is notifying
physicians, pharmacists, distributors and registered users by letter.
Blood glucose test strips used with these meters are not affected by
this notification.
More information about this notification is available on the company's
website, www.abbottdiabetescare.com
.
Jensen's Old Fashioned Smokehouse Inc. Recalls Jensen's Seattle Style Wild Smoked Salmon Spread Lemon Dill and Onion, and PCC brand Smoked Salmon Spread
Jensen's Old Fashioned Smokehouse Inc. Recalls Jensen's Seattle Style
Wild Smoked Salmon Spread Lemon Dill and Onion, and PCC brand Smoked
Salmon Spread Because of Possible Health Risk
Contact:
Mike Jensen
206-669-7590
FOR IMMEDIATE RELEASE -- Seattle, WA -- September 7, 2007 -- Jensen's
Old Fashioned Smokehouse Inc. of Seattle, WA is recalling 480 tubs of
Jensen's Seattle Style Wild Smoked Salmon Spread Lemon Dill and Onion
and 132 tubs of PCC brand Smoked Salmon Spread all-natural, because they
have the potential to be contaminated with Listeria monocytogenes, an
organism which can cause serious and sometimes fatal infections in young
children, frail or elderly people, and others with weakened immune
systems. Although healthy individuals may suffer only short-term
symptoms such as high fever, severe headache, stiffness, nausea,
abdominal pain and diarrhea, Listeria infection can cause miscarriages
and stillbirths among pregnant women.
Seattle Style Wild Smoked Salmon Spread Lemon Dill and Onion, and PCC
brand Smoked Salmon Spread all - natural were distributed in retail
stores in Western Washington.
Jensen's Seattle Style Wild Smoked Salmon Spread Lemon Dill and Onion is
coded Sell By 10/14/07 and 10/15/07, and PCC brand Smoked Salmon Spread
all-natural is coded Sell By 9/29/07. Both products were sold in 7 oz.
plastic tubs.
No illnesses have been CONFIRMED to date. The recall was the result of a
routine sampling program by the company which revealed that the finished
products contained the bacteria.
Consumers who have purchased Jensen's Seattle Style Wild Smoked Salmon
Spread Lemon Dill and Onion, and PCC brand Smoked Salmon Spread all -
natural are urged to return it to the place of purchase for a full
refund. Consumers with questions may contact the Quality Assurance
Department at Jensen's Smokehouse at 206-364-5569.
Listeria Detected in Organic Pastures Raw Cream
Listeria Detected in Organic Pastures Raw Cream
CDFA Issues Order to Withdraw Product; No Illnesses Reported
Contact:
Steve Lyle
916-654-0462
FOR IMMEDIATE RELEASE -- Sacramento, CA -- September 7, 2007 -- The
California Department of Food and Agriculture has issued an order to
Organic Pastures Dairy Company to withdraw from retail distribution
Grade A raw cream manufactured at their facility in Fresno, due to
detection of Listeria monocytogenes bacteria.
Under the recall, Organic Pastures brand Grade A raw cream with code
dates SEP 14 through SEP 21 is to be pulled immediately from retail
shelves and consumers are strongly urged to dispose of any product
remaining in their refrigerators. Until further notice, Organic Pastures
may not produce raw cream for the retail market.
The quarantine order came following laboratory confirmation of Listeria
monocytogenes bacteria. CDFA inspectors found the bacteria as a result
of product testing conducted as part of routine inspection and sample
collection at the facility.
The withdrawal order involves removal of raw cream from grocery stores,
retail outlets and farmers markets throughout California.
The great majority of cream consumed in California is pasteurized. Raw
cream is not. Pasteurization eliminates the risk of bacterial illness.
Listeria monocytogenes may cause listeriosis among "at risk" people,
including pregnant women, newborns, older adults, and people with
weakened immune systems. Symptoms include fever, muscle aches, and
sometimes nausea or diarrhea. If infection spreads to the nervous
system, symptoms such as headache and stiff neck can occur. Infected
pregnant women may experience only a mild, flu-like illness; however,
infections during pregnancy can lead to more serious problems for the
fetus. Consumers should seek immediate medical care if they develop
these symptoms.
Consumers should discard the raw cream or return it to the place of
purchase for a refund. California consumers who have purchased Organic
Pastures brand raw cream may call the company at 559- 352-6585 with
questions about the product withdrawal.
Friday, September 7, 2007
Bodee LLC, Inc. Issues A Voluntary Nationwide Recall of All Zencore Tabs, a Product Marketed as a Dietary Supplement
Bodee LLC, Inc. Issues A Voluntary Nationwide Recall of All Zencore
Tabs, a Product Marketed as a Dietary Supplement
Contact:
Bodee LLC
help@zencoretabs.com
FOR IMMEDIATE RELEASE -- Century City, CA - August 31- Bodee LLC, 2222
Avenue of the Stars, 702E, Century City, CA 90067, announced today that
it is conducting a voluntary nationwide recall of all the company's
supplement product sold under the name Zencore Tabs.
Bodee LLC is conducting this recall after being informed by
representatives of the Food and Drug Administration (FDA) that lab
analysis by FDA of Zencore Tabs samples found the product contains
potentially harmful, undeclared ingredients. FDA asserts that its
chemical analysis revealed that one lot of Zencore Tabs contains
aminotadalafil, an analog of tadalafil, the active ingredient of a
FDA-approved drug used for Erectile Dysfunction (ED). FDA maintains
Aminotadalafil is close in structure to tadalafil and is expected to
possess a similar pharmacological and adverse event profile. Further,
FDA declares another lot of Zencore Tabs contains sildenafil, the active
ingredient of another FDA-approved drug used for ED, as well as
sulfosildenafil and sulfohomosildenafil, both are analogs of sildenafil.
All of these undeclared chemicals pose a threat to consumers because
they may interact with nitrates found in some prescription drugs (such
as nitroglycerin) and may lower blood pressure to dangerous levels.
Consumers with diabetes, high blood pressure, high cholesterol, or heart
disease often take nitrates. ED is a common problem in men with these
conditions, and consumers may seek these types of products to enhance
sexual performance.
Zencore Tabs is sold in health food stores and by mail order nationwide
and in Canada. The Zencore Tabs product is sold as a 2-capsule blister
pack packaged in a retail booklet with five booklets in a box.
Customers who have this product in their possession should stop using it
immediately and contact their physician if they have experienced any
problems that may be related to taking this product.
Any adverse events that may be related to the use of this product should
be reported to the FDA's MedWatch Program by phone at 1-800-FDA-1088 or
by fax at 1-800-FDA-0178 or by mail at MedWatch, HF-2, FDA, 5600 Fishers
Lane, Rockville, MD 20852-9787.
The company advises that any unused portion be returned to Bodee LLC for
a full purchase price refund by calling (800) 935-0296 for instructions
on the return and refund process.
The Company is taking this voluntary action because it is committed and
is always concerned with the health of persons who have consumed this
product. The Company is reviewing the procedures and policies of all
firms involved with the manufacture of the product to ensure that there
will be no future issues with regard to Zencore Tabs' composition. The
Company is working closely with the FDA in the recall process and is
committed to the quality and integrity of its products. It sincerely
regrets any inconvenience to consumers and its other customers.
Tuesday, September 4, 2007
Consumer Advisory: State Agriculture Director Issues Food Safety Alert for Potato Salad
Consumer Advisory: State Agriculture Director Issues Food Safety Alert
for Potato Salad
Contact:
Communications Office
614-752-9817
FOR IMMEDIATE RELEASE -- August 31, 2007 -- Ohio Department of
Agriculture (ODA) Director Robert Boggs in conjunction with The Kroger
Co. today advises consumers not to consume Kroger brand Mustard or
Southern-Style potato salad with a "Best If Used By" date of Sept. 5,
2007, because it may contain E. coli O157:H7.
ODA's Consumer Analytical Laboratory tested a sample of the Kroger brand
Mustard or Southern-style potato salad collected during routine food
safety sampling, and found it positive for E. coli O157:H7, a foodborne
pathogen.
To date, no illnesses have been reported, and additional samples
analyzed by a certified, thirdparty laboratory contracted by Kroger have
tested negative for E. coli O157:H7. As a precautionary measure, The
Kroger Co. has removed the product from sale. The company encourages
consumers to check their refrigerators and freezers for this specific
product and, if found, to return it to the store for a full refund.
For more information regarding this product withdrawal, please visit
www.kroger.com .
Through ODA's Division of Food Safety, the department helps assure
consumers are provided foods, over-the-counter drugs, dietary
supplements, and cosmetics that are safe, unadulterated, and honestly
presented. Random, routine testing at the department's Consumer
Analytical Laboratory helps identify potentially dangerous or
adulterated products. In addition to advising consumers, the department
has notified the Food and Drug Administration and local health
departments.
for Potato Salad
Contact:
Communications Office
614-752-9817
FOR IMMEDIATE RELEASE -- August 31, 2007 -- Ohio Department of
Agriculture (ODA) Director Robert Boggs in conjunction with The Kroger
Co. today advises consumers not to consume Kroger brand Mustard or
Southern-Style potato salad with a "Best If Used By" date of Sept. 5,
2007, because it may contain E. coli O157:H7.
ODA's Consumer Analytical Laboratory tested a sample of the Kroger brand
Mustard or Southern-style potato salad collected during routine food
safety sampling, and found it positive for E. coli O157:H7, a foodborne
pathogen.
To date, no illnesses have been reported, and additional samples
analyzed by a certified, thirdparty laboratory contracted by Kroger have
tested negative for E. coli O157:H7. As a precautionary measure, The
Kroger Co. has removed the product from sale. The company encourages
consumers to check their refrigerators and freezers for this specific
product and, if found, to return it to the store for a full refund.
For more information regarding this product withdrawal, please visit
www.kroger.com
Through ODA's Division of Food Safety, the department helps assure
consumers are provided foods, over-the-counter drugs, dietary
supplements, and cosmetics that are safe, unadulterated, and honestly
presented. Random, routine testing at the department's Consumer
Analytical Laboratory helps identify potentially dangerous or
adulterated products. In addition to advising consumers, the department
has notified the Food and Drug Administration and local health
departments.
Friday, August 31, 2007
American Pie Recalls Marie Callender Turtle Pies Because of a Possible Health Risk
American Pie Recalls Marie Callender Turtle Pies Because of a Possible
Health Risk
Contact:
American Pie, LLC
1-888-339-7437, x3987
FOR IMMEDIATE RELEASE -- Woodbury, NY -- August 25, 2007 -- American
Pie, LLC, Woodbury, NY, is voluntarily recalling 1440 cases of its Marie
Callender Turtle Pies with date codes 07 (from military time 11:45 up to
and including 16:00) 143 because the product was inadvertently shipped
prior to the company obtaining satisfactory microbial test results. No
specific pathogens were found. The recall is being conducted as a
precautionary measure. Consumption of this product may lead to
gastrointestinal illness, nausea, or vomiting.
The product was shipped to the following locations:
Kroger Supermarkets: Columbus, OH; Houston, TX; Roanoke, VA; Dallas, TX;
Atlanta, GA; Memphis, TN; Shelbyville, TN; Louisville, KY;
Giant Eagle Supermarkets: Akron, Canton, Lake, Cleveland, Columbus,
Erie, Toledo, Johnston (all in Ohio); also New Castle, MD; Pittsburgh,
PA; and Youngstown, WV;
Hy-Vee Supermarkets: Iowa, Illinois, Kansas, Minnesota, Maryland,
Nebraska, and South Dakota.
There was no direct foreign distribution.
The pies are packaged in 28oz. boxes with UPC code 12781 10280.
The recall was initiated after it was discovered that the product had
been distributed without company authorization.
No illnesses have been reported to date in connection with this
situation.
Consumers who have purchased Marie Callender Turtle Pies with the above
date codes are urged to return them to the place of purchase. Consumers
with questions may contact the company at 1-888-339-7437, x3987.
Health Risk
Contact:
American Pie, LLC
1-888-339-7437, x3987
FOR IMMEDIATE RELEASE -- Woodbury, NY -- August 25, 2007 -- American
Pie, LLC, Woodbury, NY, is voluntarily recalling 1440 cases of its Marie
Callender Turtle Pies with date codes 07 (from military time 11:45 up to
and including 16:00) 143 because the product was inadvertently shipped
prior to the company obtaining satisfactory microbial test results. No
specific pathogens were found. The recall is being conducted as a
precautionary measure. Consumption of this product may lead to
gastrointestinal illness, nausea, or vomiting.
The product was shipped to the following locations:
Kroger Supermarkets: Columbus, OH; Houston, TX; Roanoke, VA; Dallas, TX;
Atlanta, GA; Memphis, TN; Shelbyville, TN; Louisville, KY;
Giant Eagle Supermarkets: Akron, Canton, Lake, Cleveland, Columbus,
Erie, Toledo, Johnston (all in Ohio); also New Castle, MD; Pittsburgh,
PA; and Youngstown, WV;
Hy-Vee Supermarkets: Iowa, Illinois, Kansas, Minnesota, Maryland,
Nebraska, and South Dakota.
There was no direct foreign distribution.
The pies are packaged in 28oz. boxes with UPC code 12781 10280.
The recall was initiated after it was discovered that the product had
been distributed without company authorization.
No illnesses have been reported to date in connection with this
situation.
Consumers who have purchased Marie Callender Turtle Pies with the above
date codes are urged to return them to the place of purchase. Consumers
with questions may contact the company at 1-888-339-7437, x3987.
Everlasting Distributors, Inc. Recalls Blue Ocean Smoked Indian Sardine Tamban Because of Possible Health Risk
Everlasting Distributors, Inc. Recalls Blue Ocean Smoked Indian Sardine
Tamban Because of Possible Health Risk
Contact:
Richard Ng
201-823-0800
FOR IMMEDIATE RELEASE -- Bayonne, NJ -- August 29, 2007 -- Everlasting
Distributors, Inc. of Bayonne, NJ, is recalling its Blue Ocean Smoked
Indian Sardine Tamban 8oz. packaged frozen products because it has the
potential to be contaminated with Clostridium botulinum, a bacterium
which can cause life-threatening illness or death. Consumers are warned
not to use the product even if it does not look or smell spoiled.
Botulism, a potentially fatal form of food poisoning, can cause the
following symptoms: general weakness, dizziness, double-vision and
trouble with speaking or swallowing. Difficulty in breathing, weakness
of other muscles, abdominal distension and constipation may also be
common symptoms. People experiencing these problems should seek
immediate medical attention.
Blue Ocean Smoked Indian Sardine Tamban was distributed in New York and
New Jersey areas and it reached consumers through retail stores.
Blue Ocean Indian Sardine Tamban comes in an uncoded white styropor foam
tray and vacuum packed with a clear plastic bag.
The potential for contamination was noted after routing testing.
No illnesses have been reported to date in connection with this problem.
Consumers who have purchased the Blue Ocean Smoked Indian Sardine Tamban
8oz. frozen product are urged to return them to the place of purchase
for a full refund. Consumers with questions may contact Everlasting
Distributors, Inc. at (201) 823-0800.
Tamban Because of Possible Health Risk
Contact:
Richard Ng
201-823-0800
FOR IMMEDIATE RELEASE -- Bayonne, NJ -- August 29, 2007 -- Everlasting
Distributors, Inc. of Bayonne, NJ, is recalling its Blue Ocean Smoked
Indian Sardine Tamban 8oz. packaged frozen products because it has the
potential to be contaminated with Clostridium botulinum, a bacterium
which can cause life-threatening illness or death. Consumers are warned
not to use the product even if it does not look or smell spoiled.
Botulism, a potentially fatal form of food poisoning, can cause the
following symptoms: general weakness, dizziness, double-vision and
trouble with speaking or swallowing. Difficulty in breathing, weakness
of other muscles, abdominal distension and constipation may also be
common symptoms. People experiencing these problems should seek
immediate medical attention.
Blue Ocean Smoked Indian Sardine Tamban was distributed in New York and
New Jersey areas and it reached consumers through retail stores.
Blue Ocean Indian Sardine Tamban comes in an uncoded white styropor foam
tray and vacuum packed with a clear plastic bag.
The potential for contamination was noted after routing testing.
No illnesses have been reported to date in connection with this problem.
Consumers who have purchased the Blue Ocean Smoked Indian Sardine Tamban
8oz. frozen product are urged to return them to the place of purchase
for a full refund. Consumers with questions may contact Everlasting
Distributors, Inc. at (201) 823-0800.
Thursday, August 30, 2007
Stirrings LLC Participates in Voluntary Nationwide Recall of Rimmer Brand Mojito Cocktail Garnish
Stirrings LLC Participates in Voluntary Nationwide Recall of Rimmer(r)
Brand Mojito Cocktail Garnish Due to Possible Health Risk from
Contaminated Raw Ingredient Supplied by Van de Vries Spice Corporation
Contact:
Paul Nardone
508-324-9800
FOR IMMEDIATE RELEASE -- Stirrings LLC, of Fall River, Massachusetts is
recalling its 3.5 oz packages of Rimmer(r) Brand Mojito Cocktail Garnish
(UPC# 80999 00046) with the best by codes 10/27/08, 10/30/08, 11/23/08,
12/01/08, 12/04/08 and 01/03/09 printed on the side of the tin. The
recall may involve approximately 5,000 cases of its Rimmer(r) Brand
Mojito Cocktail Garnish supplied by Van de Vries Spice Corporation
(formerly Atlantic Quality Spice) of Edison, NJ because they have the
potential to be contaminated with Salmonella. Although Stirrings LLC's
tests of finished product samples were negative for the presence of
Salmonella, parsley powder, one of several ingredients supplied by Van
de Vries Spice, tested positive for Salmonella.
The presence of Salmonella can cause serious and sometimes fatal
infections in young children, frail, or elderly people, and others with
weakened immune systems. Healthy persons infected with Salmonella often
experience fever, diarrhea, nausea, vomiting, and abdominal pain. In
rare circumstances, infection with Salmonella can result in the organism
getting into the bloodstream and producing more serious illnesses such
as arterial infections (i.e. infected aneurysms), endocarditis and
arthritis.
Rimmer(r) Brand Mojito Cocktail Garnish was distributed nationwide
through distributors, retail stores, internet sales and cocktail
establishments.
Immediately after Van de Vries brought to Stirrings attention that a
parsley powder used in a single lot of Mojito Rimmer product potentially
could contain Salmonella based on FDA testing, Stirrings retained expert
laboratories, primarily Shuster Laboratories of Canton, Massachusetts to
test samples of its Mojito Rimmer product for Salmonella. Testing of 24
samples drawn from the Van de Vries lot of Mojito Rimmer failed to
reveal the presence of Salmonella in the Mojito Rimmer product.
No illnesses have been reported to date.
Stirrings CEO Paul Nardone explained, "We have removed parsley powder
from our Rimmer Cocktail Garnish formula. This ingredient represents
less than one half of one percent of the blend and was used primarily as
a natural colorant." Nardone further stated, "We have initiated a recall
as a precaution and assurance to our customers that we stand behind our
product quality 100%."
Consumers who have purchased Rimmer(r) Brand Mojito Cocktail Garnish
with the best by codes noted above are asked to return it to the place
of purchase for a full refund. Consumers with questions may contact the
Company toll-free at 866-648-8239.
Brand Mojito Cocktail Garnish Due to Possible Health Risk from
Contaminated Raw Ingredient Supplied by Van de Vries Spice Corporation
Contact:
Paul Nardone
508-324-9800
FOR IMMEDIATE RELEASE -- Stirrings LLC, of Fall River, Massachusetts is
recalling its 3.5 oz packages of Rimmer(r) Brand Mojito Cocktail Garnish
(UPC# 80999 00046) with the best by codes 10/27/08, 10/30/08, 11/23/08,
12/01/08, 12/04/08 and 01/03/09 printed on the side of the tin. The
recall may involve approximately 5,000 cases of its Rimmer(r) Brand
Mojito Cocktail Garnish supplied by Van de Vries Spice Corporation
(formerly Atlantic Quality Spice) of Edison, NJ because they have the
potential to be contaminated with Salmonella. Although Stirrings LLC's
tests of finished product samples were negative for the presence of
Salmonella, parsley powder, one of several ingredients supplied by Van
de Vries Spice, tested positive for Salmonella.
The presence of Salmonella can cause serious and sometimes fatal
infections in young children, frail, or elderly people, and others with
weakened immune systems. Healthy persons infected with Salmonella often
experience fever, diarrhea, nausea, vomiting, and abdominal pain. In
rare circumstances, infection with Salmonella can result in the organism
getting into the bloodstream and producing more serious illnesses such
as arterial infections (i.e. infected aneurysms), endocarditis and
arthritis.
Rimmer(r) Brand Mojito Cocktail Garnish was distributed nationwide
through distributors, retail stores, internet sales and cocktail
establishments.
Immediately after Van de Vries brought to Stirrings attention that a
parsley powder used in a single lot of Mojito Rimmer product potentially
could contain Salmonella based on FDA testing, Stirrings retained expert
laboratories, primarily Shuster Laboratories of Canton, Massachusetts to
test samples of its Mojito Rimmer product for Salmonella. Testing of 24
samples drawn from the Van de Vries lot of Mojito Rimmer failed to
reveal the presence of Salmonella in the Mojito Rimmer product.
No illnesses have been reported to date.
Stirrings CEO Paul Nardone explained, "We have removed parsley powder
from our Rimmer Cocktail Garnish formula. This ingredient represents
less than one half of one percent of the blend and was used primarily as
a natural colorant." Nardone further stated, "We have initiated a recall
as a precaution and assurance to our customers that we stand behind our
product quality 100%."
Consumers who have purchased Rimmer(r) Brand Mojito Cocktail Garnish
with the best by codes noted above are asked to return it to the place
of purchase for a full refund. Consumers with questions may contact the
Company toll-free at 866-648-8239.
Wednesday, August 29, 2007
Metz Fresh Announces Voluntary Recall of Spinach
Metz Fresh Announces Voluntary Recall of Spinach
Contact:
Metz Fresh
831-386-1018
FOR IMMEDIATE RELEASE -- Salinas, CA -- August 28, 2007 -- Metz Fresh,
LLC is voluntarily recalling bagged spinach as a result of a positive
test for Salmonella found during routine company testing.
The spinach is distributed under the label Metz Fresh, in both retail
and food service packages. These include 10 and 16 oz bags as well as
4-2.5 lb. and 4 lb. cartons. The only Metz Fresh product affected is
spinach that bears the tracking codes 12208114, 12208214 and 12208314.
It was distributed in the continental United States and Canada.
There have been no reports of illness or problems related to this
spinach.
Salmonella is a common food borne pathogen that can cause severe
illnesses, including fever, abdominal cramps and diarrhea. While most
individuals recover in three to five days without medical intervention,
the infection can be life-threatening to young children, the elderly and
those with compromised immune systems. Consumers with any of these
symptoms should call their physician.
Consumers are advised to discard this product or return it to the place
of purchase for a refund. Consumers with questions about the recall
should contact 831-386-1018.
"Nothing is more important to Metz Fresh than the safety of our
consumers, period," said Andrew Cumming, President of Metz Fresh. "As
soon as we learned of the presumptive positive test, we directed all
customers to hold all boxes of the spinach affected as a precaution.
Now, with this positive test confirmation, there is no question that we
would recall and destroy all spinach bearing these three codes."
The positive test came during independent lab testing Metz Fresh
conducts on all of its products. Through its labeling and numbering
system, Metz Fresh has already tracked, located and put 'holds' on the
vast majority of the cartons of spinach affected. That spinach will not
be released into the marketplace.
While the positive test came from only one sample of many on three
packing lines, Metz Fresh has, as a precaution, chosen to recall all of
the spinach from the 'field lot' packed that day on all three lines.
Metz Fresh is keeping appropriate authorities updated on the status of
the voluntary recall.
Contact:
Metz Fresh
831-386-1018
FOR IMMEDIATE RELEASE -- Salinas, CA -- August 28, 2007 -- Metz Fresh,
LLC is voluntarily recalling bagged spinach as a result of a positive
test for Salmonella found during routine company testing.
The spinach is distributed under the label Metz Fresh, in both retail
and food service packages. These include 10 and 16 oz bags as well as
4-2.5 lb. and 4 lb. cartons. The only Metz Fresh product affected is
spinach that bears the tracking codes 12208114, 12208214 and 12208314.
It was distributed in the continental United States and Canada.
There have been no reports of illness or problems related to this
spinach.
Salmonella is a common food borne pathogen that can cause severe
illnesses, including fever, abdominal cramps and diarrhea. While most
individuals recover in three to five days without medical intervention,
the infection can be life-threatening to young children, the elderly and
those with compromised immune systems. Consumers with any of these
symptoms should call their physician.
Consumers are advised to discard this product or return it to the place
of purchase for a refund. Consumers with questions about the recall
should contact 831-386-1018.
"Nothing is more important to Metz Fresh than the safety of our
consumers, period," said Andrew Cumming, President of Metz Fresh. "As
soon as we learned of the presumptive positive test, we directed all
customers to hold all boxes of the spinach affected as a precaution.
Now, with this positive test confirmation, there is no question that we
would recall and destroy all spinach bearing these three codes."
The positive test came during independent lab testing Metz Fresh
conducts on all of its products. Through its labeling and numbering
system, Metz Fresh has already tracked, located and put 'holds' on the
vast majority of the cartons of spinach affected. That spinach will not
be released into the marketplace.
While the positive test came from only one sample of many on three
packing lines, Metz Fresh has, as a precaution, chosen to recall all of
the spinach from the 'field lot' packed that day on all three lines.
Metz Fresh is keeping appropriate authorities updated on the status of
the voluntary recall.
Bella Cucina Issues Allergy Alert on Undeclared Walnuts in Death by Chocolate Cookies
Bella Cucina Issues Allergy Alert on Undeclared Walnuts in Death by
Chocolate Cookies
Contact:
Bella Cucina
678-539-8400
FOR IMMEDIATE RELEASE -- Atlanta, GA -- August 27, 2007 -- Bella Cucina
of Atlanta, Georgia is recalling units of Death by Chocolate cookies if
your bag does not correctly state that the product contains walnuts.
People who have an allergy or severe sensitivity to Walnuts run the risk
of serious or life threatening allergic reaction if they consume these
products.
Death by Chocolate cookies may have been sold directly to consumers in
the following retail stores:
Store
Contact Information
Ballins, LTD
Wendy Legarde
550 Elmwood Park Blvd
Suite B
Harahan, LA 70123
At Home Store
At Home Store
Rosie Witherspoon
52 N. Main St
Fairfield, IA 52556
Perfect Package
Perfect Package
Attn:Robin
263 Park Ave
Worcester, MA 1609
USA
Lincoln Finishing Touches-NE
Lincoln Finishing Touches-NE
Attn: Linda Spurrier
3945 S. 48t
Lincoln, NE 68506
USA
Farm Fresh To You Store
Farm Fresh To You Store
Freeman O Barsotti
1 Ferry Building
Shop 9
San Francisco, CA 94105
The Fig Pantry
The Fig Pantry (bill)
Attn: Jennifer
21800 Schellville Rd
Suite C
Sonoma, CA 95476
USA
Black Salt
Black Salt
c/o:Scott Weinstein-Fish Marke
4883 MacArthur Blvd NW
Washington, DC 20007
Great American
Great American
Attn: Amy Hamilton-Hails
4121 16th Street N.
St Petersberg, FL 33703
Kiawah Island Resort
Osprey Point
Attn: Ashley Agapion Magee
700 Governors Dr.
Kiawah Island, SC 29455
Trapp & Co
Trapp & Co.
Attn: Helga/Steven
4110 Main Street
Kansas City, MO 64111
US
Joli Home and Events
Joli Home & Events
Cheryl Hunter
8B Market
Beaufort, SC 29906
James Welch
James Welch
James Welch
260 Balfour Drive
Winter Park, FL 32792
Crabby Chic
Crabby Chic
Attn: Pam Teebo
4407 Cascade Rd
Wilmington, NC 28409
McArdles Forest and Garden Center
McArdle's Forest & Garden Ctr
Attn :Sari
48 Arch Street
Greenwich, CT 6830
BCAF Grand Central Station
Bella Cucina Artful Food - GCS
1870 Murphy Avenue
Atlanta, GA 30310
Wines of Distinction, Inc.
Wines of Distinction, Inc.
Attn: Katherine Rose
230 E Main St
Abingdon, VA 24210
USA
Domaine Carneros
Domaine Carneros
Attn:Rose
1240 Duhig Road
Napa, CA 94559
Build a Basket
Build A Basket
Attn: Mena F/Scott Maybaum
32 Rte 10 West
East Hanover, NJ 07936
USA
Design Line Interiors
Design Line Interiors
Attn:Connie
4863 Shawline Street
Ste. E
San Diego, CA 92111
USA
BCAF Virginia Highlands
BCAF-Virginia Highlands
1050 North Highland Avenue
Atlanta, GA 30306
Nest
Nest
Attn: Mary Matheson
4699 South Hollady Blvd
Salt Lake City, UT 84117
Counrty Store - CA
Country Store -CA
Attn:Carol L Holmes
2408 W. Adrian Street
Newberry, CA 91320
Graeagle Gift Shop
NO CONTACT
Moravian Florist
Moravian Florist
Attn: Sue Kirchhoffer
2286 Richmond Rd.
Staten Island, NY 10306
USA
The Cheshire Cat
The Cheshire Cat
Scott Comstock
34121 N. Rt 45
Grayslake, IL 60030
Kimball Shop
Kimball Shop
Nancey Kimball
135 Main St. NE
Harbor,ME 04662
USA
Sayville General Store Inc
Sayville General Store, Inc
Attn: Jackie
44 Main Street
Sayville, NY 11782
Chintz & Company
Chintz & Company
Attn: Nicole de Goutiere
1720 Store St
Victoria, BC V8W 1V5
Canada
English Green Interiors
English Green Interiors
Attn: Deborah Green
P. O BOx 2541
Cashiers, NC 28717
Bella Donna Designs
Bella Donna Designs
Attn:Donna
131 Hurst Cir
Franklin, NC 28734
Equipment Di Vin
Equipment Di Vin
Cheryl Webster
1412 Larimer Street
Denver, CO 80202
Celebrations - FL
Celebrations-FL
Attn: Debbie
717 N. 12th Ave.
Pensacola, FL 32501
French's Kitchen & Bath
French's Kitchen & Bath
202 5th St
Hollister, CA 95023
USA
Fanciful Gift Baskets
Fanciful Gift Baskets
Attn: Dave
5617 Melrose
Los Angeles, CA 90038
Harris & Clark General Store
Harris & Clark General Store
Anissa Harris
2539 Knox St
Atlanta, Georgia 30317
Breckenridge Cheese and Chocolate
Breckenridge Cheese & Chocolate
Attn: Anne
P.O. Box 3771
Breckenridge, CO 80424
USA
Son of Moon Fine Foods
Son of the Moon
Eva Bunnell
346 South Main St.
Middletown, CT 06457
USA
Roche Bros Supermarket
Roche Bros. #101
165 Linden Street
Wellesley Hill, MA 02481
Tenzie & Co
Tenzie & Co.
1116-A Coolidge Street
Lafayette, LA 70503
USA
Pine Away
Pine Away
216 Main St.
Annapolis, MD 21401
USA
Bee Entertaining
Bee Entertaining
124 S. Webster St
Naperville, IL 60540
USA
The country Farmer
The Country Farmer
1 Bloomer Rd
N. Salem, NY 10560
All stores have been notified of the incident.
The Death by Chocolate cookies is bags are in a 6oz. bag with a sleeve
label. The UPC code for this product is 19193 00020. These cookies have
a three month shelf life. The cookies being recalled were made on June
14, 2007 and also July 5, 2007 for a total of 36 cases, 12 units per
case. The cookie ingredient list did not contain Walnuts.
No Illness have been reported to date.
Consumers should contact Bella Cucina directly at 678.539.8400 so we can
refund or replace the cookie bag.
Chocolate Cookies
Contact:
Bella Cucina
678-539-8400
FOR IMMEDIATE RELEASE -- Atlanta, GA -- August 27, 2007 -- Bella Cucina
of Atlanta, Georgia is recalling units of Death by Chocolate cookies if
your bag does not correctly state that the product contains walnuts.
People who have an allergy or severe sensitivity to Walnuts run the risk
of serious or life threatening allergic reaction if they consume these
products.
Death by Chocolate cookies may have been sold directly to consumers in
the following retail stores:
Store
Contact Information
Ballins, LTD
Wendy Legarde
550 Elmwood Park Blvd
Suite B
Harahan, LA 70123
At Home Store
At Home Store
Rosie Witherspoon
52 N. Main St
Fairfield, IA 52556
Perfect Package
Perfect Package
Attn:Robin
263 Park Ave
Worcester, MA 1609
USA
Lincoln Finishing Touches-NE
Lincoln Finishing Touches-NE
Attn: Linda Spurrier
3945 S. 48t
Lincoln, NE 68506
USA
Farm Fresh To You Store
Farm Fresh To You Store
Freeman O Barsotti
1 Ferry Building
Shop 9
San Francisco, CA 94105
The Fig Pantry
The Fig Pantry (bill)
Attn: Jennifer
21800 Schellville Rd
Suite C
Sonoma, CA 95476
USA
Black Salt
Black Salt
c/o:Scott Weinstein-Fish Marke
4883 MacArthur Blvd NW
Washington, DC 20007
Great American
Great American
Attn: Amy Hamilton-Hails
4121 16th Street N.
St Petersberg, FL 33703
Kiawah Island Resort
Osprey Point
Attn: Ashley Agapion Magee
700 Governors Dr.
Kiawah Island, SC 29455
Trapp & Co
Trapp & Co.
Attn: Helga/Steven
4110 Main Street
Kansas City, MO 64111
US
Joli Home and Events
Joli Home & Events
Cheryl Hunter
8B Market
Beaufort, SC 29906
James Welch
James Welch
James Welch
260 Balfour Drive
Winter Park, FL 32792
Crabby Chic
Crabby Chic
Attn: Pam Teebo
4407 Cascade Rd
Wilmington, NC 28409
McArdles Forest and Garden Center
McArdle's Forest & Garden Ctr
Attn :Sari
48 Arch Street
Greenwich, CT 6830
BCAF Grand Central Station
Bella Cucina Artful Food - GCS
1870 Murphy Avenue
Atlanta, GA 30310
Wines of Distinction, Inc.
Wines of Distinction, Inc.
Attn: Katherine Rose
230 E Main St
Abingdon, VA 24210
USA
Domaine Carneros
Domaine Carneros
Attn:Rose
1240 Duhig Road
Napa, CA 94559
Build a Basket
Build A Basket
Attn: Mena F/Scott Maybaum
32 Rte 10 West
East Hanover, NJ 07936
USA
Design Line Interiors
Design Line Interiors
Attn:Connie
4863 Shawline Street
Ste. E
San Diego, CA 92111
USA
BCAF Virginia Highlands
BCAF-Virginia Highlands
1050 North Highland Avenue
Atlanta, GA 30306
Nest
Nest
Attn: Mary Matheson
4699 South Hollady Blvd
Salt Lake City, UT 84117
Counrty Store - CA
Country Store -CA
Attn:Carol L Holmes
2408 W. Adrian Street
Newberry, CA 91320
Graeagle Gift Shop
NO CONTACT
Moravian Florist
Moravian Florist
Attn: Sue Kirchhoffer
2286 Richmond Rd.
Staten Island, NY 10306
USA
The Cheshire Cat
The Cheshire Cat
Scott Comstock
34121 N. Rt 45
Grayslake, IL 60030
Kimball Shop
Kimball Shop
Nancey Kimball
135 Main St. NE
Harbor,ME 04662
USA
Sayville General Store Inc
Sayville General Store, Inc
Attn: Jackie
44 Main Street
Sayville, NY 11782
Chintz & Company
Chintz & Company
Attn: Nicole de Goutiere
1720 Store St
Victoria, BC V8W 1V5
Canada
English Green Interiors
English Green Interiors
Attn: Deborah Green
P. O BOx 2541
Cashiers, NC 28717
Bella Donna Designs
Bella Donna Designs
Attn:Donna
131 Hurst Cir
Franklin, NC 28734
Equipment Di Vin
Equipment Di Vin
Cheryl Webster
1412 Larimer Street
Denver, CO 80202
Celebrations - FL
Celebrations-FL
Attn: Debbie
717 N. 12th Ave.
Pensacola, FL 32501
French's Kitchen & Bath
French's Kitchen & Bath
202 5th St
Hollister, CA 95023
USA
Fanciful Gift Baskets
Fanciful Gift Baskets
Attn: Dave
5617 Melrose
Los Angeles, CA 90038
Harris & Clark General Store
Harris & Clark General Store
Anissa Harris
2539 Knox St
Atlanta, Georgia 30317
Breckenridge Cheese and Chocolate
Breckenridge Cheese & Chocolate
Attn: Anne
P.O. Box 3771
Breckenridge, CO 80424
USA
Son of Moon Fine Foods
Son of the Moon
Eva Bunnell
346 South Main St.
Middletown, CT 06457
USA
Roche Bros Supermarket
Roche Bros. #101
165 Linden Street
Wellesley Hill, MA 02481
Tenzie & Co
Tenzie & Co.
1116-A Coolidge Street
Lafayette, LA 70503
USA
Pine Away
Pine Away
216 Main St.
Annapolis, MD 21401
USA
Bee Entertaining
Bee Entertaining
124 S. Webster St
Naperville, IL 60540
USA
The country Farmer
The Country Farmer
1 Bloomer Rd
N. Salem, NY 10560
All stores have been notified of the incident.
The Death by Chocolate cookies is bags are in a 6oz. bag with a sleeve
label. The UPC code for this product is 19193 00020. These cookies have
a three month shelf life. The cookies being recalled were made on June
14, 2007 and also July 5, 2007 for a total of 36 cases, 12 units per
case. The cookie ingredient list did not contain Walnuts.
No Illness have been reported to date.
Consumers should contact Bella Cucina directly at 678.539.8400 so we can
refund or replace the cookie bag.
Monday, August 27, 2007
Revised: FDA Expands Warning on Eating Raw Oysters from Hood Canal in Washington State
This release was updated on August 27, 2007 to include additional areas of distribution.
FDA News
FOR IMMEDIATE RELEASE
August 24, 2007
Media Inquiries:
Michael Herndon, 301-827-6242
Consumer Inquiries:
888-INFO-FDA
FDA Expands Warning on Eating Raw Oysters from
Hood Canal in Washington State
Additional Growing Area Linked to Illness Outbreaks
The U.S. Food and Drug Administration is warning consumers not to eat raw oysters harvested from an additional part (growing area 5) of the southern tip of Hood Canal in Washington state due to a foodborne illness outbreak caused by Vibrio parahaemolyticus bacteria. This follows an earlier outbreak and August 10 warning about oysters harvested from growing area 6 of Hood Canal.
Symptoms of the illness, vibriosis, include watery diarrhea, often with abdominal cramping, nausea, vomiting, fever, and chills. Usually these symptoms occur within 24 hours of ingestion and last no more than three days. Severe disease is rare and occurs most commonly in people with weakened immune systems. Those who believe they have experienced these symptoms after consuming raw oysters should consult their health care provider and contact their local health department.
Raw oysters harvested from growing area 5 in Hood Canal from July 31 through August 20, 2007 have caused at least six people to become ill in Washington state. To date, records indicate that raw oysters from the area were distributed to Arizona, California, Colorado, Delaware, Florida, Idaho, Minnesota, New York, Oregon, Pennsylvania, Utah, Washington state, British Columbia (Canada). Bali (Indonesia), Hong Kong, Singapore, and Thailand.
The Washington State Department of Health has closed the growing area associated with the illness and has asked commercial oyster harvesters and dealers who obtained oysters from this area to recall them.
Consumers who have recently purchased oysters should check with the place of purchase and ask if they were harvested from the affected growing areas. The recall involves both shucked oysters and oyster in the shell (shell stock oysters).
Those with weakened immune systems, including people affected by HIV/AIDS, chronic alcohol abuse, liver, stomach, or blood disorders, cancer, diabetes, or kidney disease, should avoid eating raw oysters, regardless of where they are harvested.
FDA advises that consumers can continue to enjoy oysters in many cooked preparations by doing the following:
At Restaurants and other Foodservice Establishments:
* Order oysters fully cooked.
In the Shell:
* Purchase oysters with the shells closed
* Throw away any oysters with shells already opened.
* Never allow raw seafood to come into contact with cooked food.
* Boil or steam the oysters:
* Boil oysters until the shells open. Once shells open, boil for an additional three to five minutes.
* To steam-add oysters to water that is already steaming and cook live oysters until the shells open, once open steam for another four to nine minutes.
* Use smaller pots to boil or steam oysters. Using larger pots, or cooking too many oysters at one time,
* Discard any oysters that do not open during cooking.
Shucked Oysters:
* Never allow raw seafood to come into contact with cooked food.
* Cook the oysters in one of the following ways:
* Boil or simmer shucked oysters for at least three minutes or until the edges curl. \
* Fry at 375° F for at least three minutes.
* Broil three inches from heat for three minutes.
* Bake at 450° F for 10 minutes.
For more information:
Hood canal oyster area closed - second closure due to illness outbreak
www.doh.wa.gov/Publicat/2007_news/07-143.htm
FDA News
FOR IMMEDIATE RELEASE
August 24, 2007
Media Inquiries:
Michael Herndon, 301-827-6242
Consumer Inquiries:
888-INFO-FDA
FDA Expands Warning on Eating Raw Oysters from
Hood Canal in Washington State
Additional Growing Area Linked to Illness Outbreaks
The U.S. Food and Drug Administration is warning consumers not to eat raw oysters harvested from an additional part (growing area 5) of the southern tip of Hood Canal in Washington state due to a foodborne illness outbreak caused by Vibrio parahaemolyticus bacteria. This follows an earlier outbreak and August 10 warning
Symptoms of the illness, vibriosis, include watery diarrhea, often with abdominal cramping, nausea, vomiting, fever, and chills. Usually these symptoms occur within 24 hours of ingestion and last no more than three days. Severe disease is rare and occurs most commonly in people with weakened immune systems. Those who believe they have experienced these symptoms after consuming raw oysters should consult their health care provider and contact their local health department.
Raw oysters harvested from growing area 5 in Hood Canal from July 31 through August 20, 2007 have caused at least six people to become ill in Washington state. To date, records indicate that raw oysters from the area were distributed to Arizona, California, Colorado, Delaware, Florida, Idaho, Minnesota, New York, Oregon, Pennsylvania, Utah, Washington state, British Columbia (Canada). Bali (Indonesia), Hong Kong, Singapore, and Thailand.
The Washington State Department of Health has closed the growing area associated with the illness and has asked commercial oyster harvesters and dealers who obtained oysters from this area to recall them.
Consumers who have recently purchased oysters should check with the place of purchase and ask if they were harvested from the affected growing areas. The recall involves both shucked oysters and oyster in the shell (shell stock oysters).
Those with weakened immune systems, including people affected by HIV/AIDS, chronic alcohol abuse, liver, stomach, or blood disorders, cancer, diabetes, or kidney disease, should avoid eating raw oysters, regardless of where they are harvested.
FDA advises that consumers can continue to enjoy oysters in many cooked preparations by doing the following:
At Restaurants and other Foodservice Establishments:
* Order oysters fully cooked.
In the Shell:
* Purchase oysters with the shells closed
* Throw away any oysters with shells already opened.
* Never allow raw seafood to come into contact with cooked food.
* Boil or steam the oysters:
* Boil oysters until the shells open. Once shells open, boil for an additional three to five minutes.
* To steam-add oysters to water that is already steaming and cook live oysters until the shells open, once open steam for another four to nine minutes.
* Use smaller pots to boil or steam oysters. Using larger pots, or cooking too many oysters at one time,
* Discard any oysters that do not open during cooking.
Shucked Oysters:
* Never allow raw seafood to come into contact with cooked food.
* Cook the oysters in one of the following ways:
* Boil or simmer shucked oysters for at least three minutes or until the edges curl. \
* Fry at 375° F for at least three minutes.
* Broil three inches from heat for three minutes.
* Bake at 450° F for 10 minutes.
For more information:
Hood canal oyster area closed - second closure due to illness outbreak
www.doh.wa.gov/Publicat/2007_news/07-143.htm
Saturday, August 25, 2007
Mars Petcare US, Inc. Recalls Dry Dog Food
FDA News
FOR IMMEDIATE RELEASE
August 25, 2007
Media Inquiries:
Michael Herndon, 301-827-6242
Consumer Inquiries:
888-INFO-FDA
Mars Petcare US, Inc. Recalls Dry Dog Food
The U.S. Food and Drug Administration is alerting consumers that Mars
Petcare US, Inc. has recalled two dry dog food products because of the
potential contamination with Salmonella Schwarzengrund.
The Mars Petcare US, based in Franklin, Tenn. is voluntarily recalling
five-pound bags of Krasdale Gravy dry dog food sold in Connecticut,
Massachusetts, New Jersey, New York, and Pennsylvania, and 50-pound bags
of Red Flannel Large Breed Adult Formula dry food sold in Pennsylvania.
The FDA conducted tests on 10 samples, representing seven product brands
from the company. Each sample (same size and brand of product) consisted
of 15 subsamples, for a total of 150 subsamples. Tests of the 150
subsamples revealed two positive samples; one from the Krasdale Gravy
dry food and another from Red Flannel Large Breed Adult Formula dry
food.
Salmonella can potentially be transferred to people handling pet food,
especially if they have not thoroughly washed their hands after having
contact with the product or any surfaces exposed to the product. To
date, there have been 64 cases of illness in humans related to
Salmonella Schwarzengrund reported to the U.S. Centers for Disease
Control and Prevention (CDC); however, none of the reported cases have
been directly linked to the recalled product that was tested. The FDA is
working with local and state officials, and with officials at the CDC in
the investigation.
Here is identification information on the recalled products:
Product: Krasdale Gravy dry dog food
Size: Five-pound bag
UPC Code: 7513062596
Best By Date: July 16, 2008 & July 17, 2008
Best By Date Location: Back of bag
Distribution: Stores in Connecticut, Massachusetts, New Jersey, New
York, and Pennsylvania
Product: Red Flannel Large Breed Adult Formula dry dog food
Size: 50-pound bag
UPC Code: 4286900062
Best By Date: July 12, 2008
Best By Date Location: Back of bag
Distribution: Stores in Reedsland and Richlandtown, Pa.
Salmonella is an organism which can cause serious and sometimes fatal
infections in young children, frail or elderly people, and others with
weakened immune systems. Healthy persons infected with Salmonella often
experience fever, diarrhea (which may be bloody), nausea, vomiting and
abdominal pain. In rare circumstances, infection with Salmonella can
result in the organism getting into the bloodstream and producing more
severe illnesses such as arterial infections (i.e., infected aneurysms),
endocarditis and arthritis.
Pets with Salmonella infections may be lethargic and have diarrhea or
bloody diarrhea, fever, and vomiting. Some pets will have only decreased
appetite, fever and abdominal pain. Well animals can be carriers and
infect other animals or humans. If your pet has consumed the recalled
product and has these symptoms, please contact your veterinarian.
Consumers with questions about the recalled product should call Mars
Petcare US, Inc. at 866-298-8332.
For more information:
Safe Handling Tips for Pet Foods and Treats
FOR IMMEDIATE RELEASE
August 25, 2007
Media Inquiries:
Michael Herndon, 301-827-6242
Consumer Inquiries:
888-INFO-FDA
Mars Petcare US, Inc. Recalls Dry Dog Food
The U.S. Food and Drug Administration is alerting consumers that Mars
Petcare US, Inc. has recalled two dry dog food products because of the
potential contamination with Salmonella Schwarzengrund.
The Mars Petcare US, based in Franklin, Tenn. is voluntarily recalling
five-pound bags of Krasdale Gravy dry dog food sold in Connecticut,
Massachusetts, New Jersey, New York, and Pennsylvania, and 50-pound bags
of Red Flannel Large Breed Adult Formula dry food sold in Pennsylvania.
The FDA conducted tests on 10 samples, representing seven product brands
from the company. Each sample (same size and brand of product) consisted
of 15 subsamples, for a total of 150 subsamples. Tests of the 150
subsamples revealed two positive samples; one from the Krasdale Gravy
dry food and another from Red Flannel Large Breed Adult Formula dry
food.
Salmonella can potentially be transferred to people handling pet food,
especially if they have not thoroughly washed their hands after having
contact with the product or any surfaces exposed to the product. To
date, there have been 64 cases of illness in humans related to
Salmonella Schwarzengrund reported to the U.S. Centers for Disease
Control and Prevention (CDC); however, none of the reported cases have
been directly linked to the recalled product that was tested. The FDA is
working with local and state officials, and with officials at the CDC in
the investigation.
Here is identification information on the recalled products:
Product: Krasdale Gravy dry dog food
Size: Five-pound bag
UPC Code: 7513062596
Best By Date: July 16, 2008 & July 17, 2008
Best By Date Location: Back of bag
Distribution: Stores in Connecticut, Massachusetts, New Jersey, New
York, and Pennsylvania
Product: Red Flannel Large Breed Adult Formula dry dog food
Size: 50-pound bag
UPC Code: 4286900062
Best By Date: July 12, 2008
Best By Date Location: Back of bag
Distribution: Stores in Reedsland and Richlandtown, Pa.
Salmonella is an organism which can cause serious and sometimes fatal
infections in young children, frail or elderly people, and others with
weakened immune systems. Healthy persons infected with Salmonella often
experience fever, diarrhea (which may be bloody), nausea, vomiting and
abdominal pain. In rare circumstances, infection with Salmonella can
result in the organism getting into the bloodstream and producing more
severe illnesses such as arterial infections (i.e., infected aneurysms),
endocarditis and arthritis.
Pets with Salmonella infections may be lethargic and have diarrhea or
bloody diarrhea, fever, and vomiting. Some pets will have only decreased
appetite, fever and abdominal pain. Well animals can be carriers and
infect other animals or humans. If your pet has consumed the recalled
product and has these symptoms, please contact your veterinarian.
Consumers with questions about the recalled product should call Mars
Petcare US, Inc. at 866-298-8332.
For more information:
Safe Handling Tips for Pet Foods and Treats
Thursday, August 23, 2007
Los Angeles Salad Company Voluntarily Recalls Product Because of Possible Health Risk
Los Angeles Salad Company Voluntarily Recalls Product Because of
Possible Health Risk
Contact:
John Shaughnessy
626-322-9017
FOR IMMEDIATE RELEASE -- Industry, CA -- August 22, 2007 -- Los Angeles
Salad Company, located in City of Industry, CA is recalling its "Genuine
Sweet Baby Carrots" with a Sell By Date Code up to and including August
16, 2007 printed on the back of the packages because the product may be
contaminated with the bacteria Shigella. Shigella infection can cause
diarrhea (which may be bloody), fever, nausea and vomiting. Illness
usually lasts from 4 to 14 days. In some persons, especially the very
young, the very old and people with compromised immune systems, the
diarrhea can be more severe. Infection can occur after eating and
drinking food and water that is contaminated with Shigella and can be
passed from person to person.
The product was sold in packages with two labels. One is labeled "Los
Angeles Salad Genuine Sweet Baby Carrots" distributed by Kroger Co. King
Sooper, in Colorado, Kroger Co. Ralphs in California; Publix in Georgia
and Florida. All of these packages were sold in flexible plastic bags in
7 and 8 oz. size with a Sell By Date Code up to and including August 16,
2007. The second label was "Trader Joe's Genuine Sweet Baby Carrots"
distributed by Trader Joe's in Arizona, California, New Mexico, Nevada,
Oregon and Washington in 7 oz. flexible plastic bags with a Sell By Date
Code up to and including August 8, 2007.
The recall was initiated after it was discovered that the same product
sold in Canada was contaminated with Shigella. There were four reported
incidences of illness in Canada from August 4-6, 2007. No one was
hospitalized and all persons affected have fully recovered. An ongoing
investigation is being conducted to find the cause of the problem, but
at this time the source has not been determined.
This is precautionary notice. Consumers who have purchased Los Angeles
Salad Company's "Genuine Sweet Baby Carrots" are urged to return it to
the place of purchase for a full refund. Consumers with questions may
contact Los Angeles Salads at (1-626-322-9017).
Possible Health Risk
Contact:
John Shaughnessy
626-322-9017
FOR IMMEDIATE RELEASE -- Industry, CA -- August 22, 2007 -- Los Angeles
Salad Company, located in City of Industry, CA is recalling its "Genuine
Sweet Baby Carrots" with a Sell By Date Code up to and including August
16, 2007 printed on the back of the packages because the product may be
contaminated with the bacteria Shigella. Shigella infection can cause
diarrhea (which may be bloody), fever, nausea and vomiting. Illness
usually lasts from 4 to 14 days. In some persons, especially the very
young, the very old and people with compromised immune systems, the
diarrhea can be more severe. Infection can occur after eating and
drinking food and water that is contaminated with Shigella and can be
passed from person to person.
The product was sold in packages with two labels. One is labeled "Los
Angeles Salad Genuine Sweet Baby Carrots" distributed by Kroger Co. King
Sooper, in Colorado, Kroger Co. Ralphs in California; Publix in Georgia
and Florida. All of these packages were sold in flexible plastic bags in
7 and 8 oz. size with a Sell By Date Code up to and including August 16,
2007. The second label was "Trader Joe's Genuine Sweet Baby Carrots"
distributed by Trader Joe's in Arizona, California, New Mexico, Nevada,
Oregon and Washington in 7 oz. flexible plastic bags with a Sell By Date
Code up to and including August 8, 2007.
The recall was initiated after it was discovered that the same product
sold in Canada was contaminated with Shigella. There were four reported
incidences of illness in Canada from August 4-6, 2007. No one was
hospitalized and all persons affected have fully recovered. An ongoing
investigation is being conducted to find the cause of the problem, but
at this time the source has not been determined.
This is precautionary notice. Consumers who have purchased Los Angeles
Salad Company's "Genuine Sweet Baby Carrots" are urged to return it to
the place of purchase for a full refund. Consumers with questions may
contact Los Angeles Salads at (1-626-322-9017).
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