FDA posts press releases and other notices of recalls 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.


American Spice Company Inc. Recalls Ground Cumin
2 oz. Lot # 03162002 Because of Possible Health Risk

NEWS RELEASE



Contact:  American Spice Company Inc.
          305-326-0900 ext. 121
                

For Immediate Release

American Spice Company Inc. Recalls Ground Cumin 2 Oz. Lot # 03162002 Because of Possible Health Risk

Miami, FL - August 27, 2002 -- American Spice Company Inc. of Miami Fl. is recalling Ground Cumin 2 oz. bottles bearing LOT # 03162002 because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstance, 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), endocarditic and arthritis.

The Ground Cumin 2 oz. bearing lot # 03162002 was distributed to retail supermarkets and distributors in South Florida.

The Ground Cumin is packed in a 2 oz. clear plastic bottle Brand Name American Spice Company Inc. bearing LOT # 03162002 and expiration date of 3/16/05.

No illnesses have been reported to date.

The recall was as the result of a routine sampling program by FDA which revealed that the finished products contained the bacteria. American Spice has ceased the production and distribution of the product as FDA and American Spice continue their investigation as to what caused the problem.

Consumers who have purchased American Spice Brand Ground Cumin 2 oz. are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the American Spice Company at 305-326-0900 (Ext: 121.)



Recalls Home | FDA Home Page | Search | A-Z Index | Site Map | Contact FDA

FDA/Website Management Staff
Web page created by tg 2002-AUG-28.