FDA Recalls 3 Dietary Supplements Due to Potential Salmonella

(July 12, 2012)

The U.S. Food and Drug Administration (FDA) notified consumers and healthcare professionals of a recall of three dietary supplements due to potential salmonella contamination.

The three recalled dietary supplements are:

  • Cataplex ACP (product #0700 & 0750) Lot 114
  • Cataplex C (product #1650 & 1655) Lot 114
  • Pancreatrophin PMG (product #6650) Lot 114

This recall resulted during a routine FDA record inspection, which revealed that one of the ingredients used in these products potentially contained the bacteria. Salmonella is an organism, which can cause serious and sometimes fatal infections in young children, frail or elderly people, and those with weakened or compromised immune systems. The products, all tablets, were distributed in 60 cc. and 200 cc. amber glass bottles with “Best Used by Dates” 5/13 on boxes and bottles. They were sold to consumers through healthcare professionals.

If you believe you have purchased one of these recalled products, you may be entitled to compensation. Contact one of our Gacovino Lake & Associates attorneys at 1-800-246-HURT (4878).

Related Posts