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SafetyAlerts
March 05, 2003

Schering-Plough Has Recalled Feen-A-Mint Tablets

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

PRODUCT
Feen-A-Mint Tablets, Laxative, (Bisacodyl ) 5mg, 10 tablet carton.
Recall # D-140-3.

CODE
1-EGN-4, EXP 1/3.

RECALLING FIRM/MANUFACTURER
Schering-Plough HealthCare Products/DBA Bain deSoleil Co., Cleveland, TN,
by letter dated December 10, 2002. Firm initiated recall ongoing.

REASON
Disintegration: failure due to tablet softening.

VOLUME OF PRODUCT IN COMMERCE
109,728 packages.

DISTRIBUTION
Nationwide.

 

 
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During 2000 there were over
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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.