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PRODUCT
Carisoprodol Tablets, USP, 350mg, 500 and 1000 tablet bottles. Recall # D-221-3.
CODE
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.
RECALLING FIRM/MANUFACTURER
Able Laboratories, Inc., South Plainfield, NJ, by letter dated January 15, 2003. Firm initiated recall is ongoing.
REASON
Incorrect tablet imprinting; some tablets bear the incorrect identification "A265" rather than "A266".
VOLUME OF PRODUCT IN COMMERCE
7,731 bottles.
DISTRIBUTION
Nationwide.

http://www.fda.gov/bbs/topics/enforce/2003/ENF00793.html

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