September 4, 2002
Alliance Has Recalled Zerit (stavudine) Capsules
- The Food and Drug Administration (FDA)
has released the
Zerit (stavudine) Capsules, 40 mg, bottles of 60, Rx only. Recall # D-398-2.
Lot 1A36209, Exp. FEB 2003.
Recalling Firm: Alliance Wholesale Distributor, Richton Park, IL, by letter
dated June 28, 2002.
Manufacturer: Bristol-Myers Squibb Oncology/Immunology, Princeton, NJ. Firm
initiated recall is ongoing.
Tablets changed to capsules.
VOLUME OF PRODUCT IN COMMERCE