 |
 |
 |
|
 |
FDA Home Page | Search FDA Site | FDA A-Z Index | Contact FDA
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.
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:
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.
RSS Feed for FDA Recalls Information [what's this?]
Get free e-mail alerts about Class I recalls