April 30, 2003
Able Laboratories Has Recalled
The Food and Drug
Administration (FDA) released the following information.
Carisoprodol Tablets, USP, 350mg, 500 and 1000 tablet bottles. Recall #
1,000 tablet bottles -- 210049A exp. 9/04;
210050A exp. 9/04;
500 tablet bottles -- 210051A exp. 9/04;
210052A exp. 9/04; 210053A exp 10/04.
Able Laboratories, Inc., South Plainfield, NJ, by letter dated January 15,
2003. Firm initiated recall is ongoing.
Incorrect tablet imprinting; some tablets bear the incorrect identification
"A265" rather than "A266".
VOLUME OF PRODUCT IN COMMERCE