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
Friday, September 28, 2007
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.
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