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Safety Alerts
August 4, 1999

Thompson Medical Company, Inc. Recalls Quick Pep® Alertness Aid Tablets

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).

PRODUCT
Quick Pep® Alertness Aid Tablets, 150 mg caffeine anhydrous, USP, 32 tablet units, OTC indicated as a stimulant.NDC #11926-006-32.

Recall #D-294-9.

CODE
Lot Numbers: SQP196A and SQP796A.

MANUFACTURER
Sidmak Laboratories, E. Hanover, New Jersey.

RECALLED BY
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.

DISTRIBUTION
Nationwide.

QUANTITY
59,940 cartons were distributed.

 

The information contained herein has been obtained from sources that the Company believes to be reliable, however, the Company has not independently verified or confirmed the information and the recipient acknowledges that no representations or warranties are being made in connection with the use of the information.