October 10, 2002
Recall Update: Pharmaceutical Corp
Allegra 60 mg Recall Complete
The Food and Drug
Administration (FDA) released the following information.
Allegra 60 mg (Fexofenadine HCl Capsules), 14 and 60 count bottles, Rx only.
Recall # D-001-3.
Lot no. 1044325, exp. 5/2004 and
Lot no. 1048818, exp. 10/2004.
Recalling Firm: Pharmaceutical Corp. of America, Indianapolis, IN, by phone
on September 10, 2002.
Manufacturer: Aventis Pharmaceuticals, Inc., Kansas City, MO. Firm initiated
recall is complete.
Label mixup; bottles labeled as containing 60mg capsules actually contain
VOLUME OF PRODUCT IN COMMERCE
CA and MI.