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SafetyAlerts
February 7, 2003

Bristol-Myers Squibb Has Recalled ESTRACE tablets

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

PRODUCT
ESTRACE tablets (estradiol tablets, USP), 2 mg, 100 and 500 count bottles, Rx Only. Recall # D-116-3.

CODE
100 Count bottles - Lot no. 0K28404, Exp. Date Oct-2003, 500 Count bottles - Lot no. 0J41630, Exp. Date Oct-2003.

RECALLING FIRM/MANUFACTURER
Bristol-Myers Squibb Company, New Brunswick, NJ, by letters on November 11, 2002. Firm initiated recall is ongoing.

REASON
Dissolution Failure.

VOLUME OF PRODUCT IN COMMERCE
4,587 bottles.

DISTRIBUTION
Nationwide and Canada.

 

 
Selected Recent Recalls


Health Professional:

Did you know?
During 2000 there were over
1050 products recalled in the United
States for safety reasons!

How many did you hear about?

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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.