Action Labs, Inc. Conducts Recall of Shark Cartilage Capsules Because of Possible Health Risk
Posted by
RLF StaffJune 12, 2007 6:10 AMAction Labs, Inc. of Anaheim, CA, is voluntarily recalling its Sentinel brand Shark Cartilage Capsules manufactured in 2005 because they have 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 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.
Routine testing performed recently at NBTY, Inc. (the manufacturer) shows that the recalled capsules have the potential to be contaminated with Salmonella. Although multiple lot numbers may have been involved in the recall by NBTY, only NBTY lot number 64951 was purchased, repacked and distributed by Action Labs, Inc.
The Shark Cartilage Capsules were sold in bottles of 60 capsules and labeled as Sentinel Shark Cartilage 750mg. A sticker with lot number 064951 and expiration date 07 2009 is located on the bottom of the bottle. The Shark Cartilage Capsules were distributed to retail establishments in Southern California and internationally to Hong Kong.
No illnesses have been reported to date. This recall is being made with the knowledge of the US Food and Drug Administration.
Customers may return product to the place of purchase for a full refund. Customers may also contact the company with questions and to obtain information on how to return the product at 1-714-630-5941.