August 8, 2002
Berlex Laboratories Has Recalled Quinaglute Dura-Tabs
- The FDA has released the following information.
Quinaglute Dura-Tabs, Extended Release Tablets (quinidine gluconate, USP)
324 mg, 100, 250, and 500 count bottles, Rx. Recall # D-370-2.
W00238 Exp. 11/2004
W00239 Exp. 12/2004
W00240 Exp. 1/2005
W10001 Exp. 3/2005
W10028 Exp. 4/2005
W10029 Exp. 5/2005
W10111 Exp. 7/2005.
Berlex Laboratories, Inc., Wayne, NJ, by letters on July 23, 2002.
Firm initiated recall is ongoing.
Metal particles in tablets.
VOLUME OF PRODUCT IN COMMERCE
2,603 bottles of 100's; 3,358 bottles of 250's; 15,286 bottles of 500's.