Medical Company, Inc. Recalls Quick Pep® Alertness Aid Tablets
August 4, 1999
Fairfield, NJ (SafetyAlerts) - The Food and Drug
Administration (FDA) today reported that Thompson Medical Company, Inc. is recalling Quick
Pep® Alertness Aid Tablets because of mislabeling. The blister card incorrectly
declares caffeine anhydrous, USP, Strength as 200 mg (outer holding cartoncorrectly
labeled as 150 mg).
Quick Pep® Alertness Aid Tablets, 150 mg caffeine
anhydrous, USP, 32 tablet units, OTC indicated as a stimulant.NDC #11926-006-32.
Lot Numbers: SQP196A and SQP796A.
Sidmak Laboratories, E. Hanover, New Jersey.
Thompson Medical Company, Inc., Fairfield, New Jersey, by letter mailed on January
26 and 27, 1999, February 15, 1999, and April 7, 1999. Firm-initiated recall complete.
59,940 cartons were distributed.