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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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