March 29, 2002Aventis Pharmaceuticals Allegra Recall
- The Food and Drug Administration (FDA) has released the following
Allegra tablets (fexofenadine HCl) 60 mg., 2-tablet blister
packages (30-ct. boxes)physician samples, Rx Only
The responsible firm on the label is Aventis Pharmaceuticals Inc., Kansas
City, MO. Recall # D-212-2.
Lot 1027124, exp. 2/3/03
Lot 1027842, exp. 2/3/03
Lot 1028789, exp. 2/4/03.
Aventis Pharmaceuticals, Inc. Kansas City, MO, by e-mail dated July 3, 2001.
FDA initiated recall is complete.
Product was not manufactured in conformance with its New Drug Application (NDA)
specifications, lacking particle size and friability testing
VOLUME OF PRODUCT IN COMMERCE