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.
Tuesday, October 30, 2007
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.
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