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SafetyAlerts
April 30, 2003

Able Laboratories Has Recalled Carisoprodol Tablets

(SafetyAlerts) - The Food and Drug Administration (FDA) released the following information.

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
.

 
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The information contained herein has been obtained from sources that the Company believes to be reliable, however, the Company has not independently verified or confirmed the information and the recipient acknowledges that no representations or warranties are being made in connection with the use of the information.