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SafetyAlerts
February 8, 2000

Med-Pro, Inc. Recalls Esgic-Plus Tablets

Lexington, NE (SafetyAlerts) - The Food and Drug Administration (FDA) today reported that Med-Pro, Inc. is recalling Esgic-Plus Tablets because the bottles contain capsule form of the same ingredient product, not the labeled tablet form of product.

The recalled Esgic-Plus Tablets (butalbital 50mg, acetaminophen 500mg, caffeine 40mg), was sold in 100 tablet bottles (NDC #0456-0618-01) and distributed in New York.

According to FDA, 999 bottles were distributed and can be identified by the Lot Number #90248A 1 EXP 8/01

This ongoing Class III recall was initiated by Med-Pro, Inc. by fax on December 27, 1999.  This is the first public notice issued by the FDA.

Questions concerning this recall may be directed to the FDA at 1-888-INFO-FDA.
FDA Recall D-210-0

 
Selected Recent Recalls


Health Professional:

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

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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.