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.
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