September 4, 2002
AmeriSource Health Services Has Recalled
- The Food and Drug Administration (FDA)
has released the
Quinaglute (quinidine gluconate, USP), Dura-Tabs (extended-release tablets,
USP) 324 mg, 100 count bottles, Rx only. Recall # D-399-2.
Lot #012634, Exp. OCT 23 03
Lot #012831, Exp. NOV 27 03
Lot #012263, Exp. SEP 04 03.
Recalling Firm: AmeriSource Health Services Corp., Columbus, OH, by letter
and fax on August 20, 2002.
Manufacturer: Berlex Laboratories, Wayne, NJ. Firm initiated recall is
Metal particles found in tablet (by manufacturer).
VOLUME OF PRODUCT IN COMMERCE
687 bottles total.