July 17, 2002
Alliance Wholesale Distributor Has Recalled
- The Food and Drug Administration (FDA) has released the following
Combivir Tablets (lamivudine 150 mg/zidovudine 300 mg) 60 tablet bottles,
NDC #0173-0595-00, GlaxoWellcome.
Recall # D-350-2.
Lots 1ZP0848, 1ZP2346, 1ZP2347.
Recalling Firm: Alliance Wholesale Distributor, Richton Park, IL, by
telephone on May 10, 2002. Manufacturer:
Unknown. Firm initiated recall is ongoing.
Counterfeit: bottles labeled to contain Combivir tablets may contain Ziagen
VOLUME OF PRODUCT IN COMMERCE
IL, CA, IN, NY, TN, PA, MD and NJ.