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SafetyAlerts
September 4, 2002

Alliance Has Recalled Zerit (stavudine) Capsules

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

PRODUCT
Zerit (stavudine) Capsules, 40 mg, bottles of 60, Rx only. Recall # D-398-2.

CODE
Lot 1A36209, Exp. FEB 2003.

RECALLING FIRM/MANUFACTURER
Recalling Firm: Alliance Wholesale Distributor, Richton Park, IL, by letter dated June 28, 2002.
Manufacturer: Bristol-Myers Squibb Oncology/Immunology, Princeton, NJ. Firm initiated recall is ongoing.

REASON
Tablets changed to capsules.

VOLUME OF PRODUCT IN COMMERCE
26 bottles.

DISTRIBUTION
Nationwide.

 
Selected Recent Recalls


Health Professional:

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During 2000 there were over
1050 products recalled in the United
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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.