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11/20/03 at 5:17pm
Thread Starter 
(SafetyAlerts) - The FDA has released the following information.

PRODUCT
Actifed Cold & Allergy tablets (60 mg Pseudoephedrine HCl, 2.5 mg Triprolidine HCl), 12 count blister/carton. Recall # D-062-4.

CODE
Lot No. Exp. Date 24112V 10/2005 15952V 6/2005.

RECALLING FIRM/MANUFACTURER
Pfizer Inc., Morris Plains, NJ, by letter on October 1, 2003. Firm initiated recall is ongoing.

REASON
Misbranding; some of the dosing information and/or ingredient listing information may be missing from the carton.

VOLUME OF PRODUCT IN COMMERCE
666,678.

DISTRIBUTION
Nationwide.
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