December 28, 1999Textilease
Medique, Inc. Recalls Medi-First Extra Strength Non-Aspirin Acetaminophen
Skokie, IL (SafetyAlerts) - The Food and Drug
Administration (FDA) today reported that Textilease Medique, Inc. is recalling Medi-First
Extra Strength Non-Aspirin Acetaminophen because of mislabeling. The exterior
holding/dispensing cartons labeled as non-aspirin ibuprofen 200 mg.
This ongoing Class III recall was initiated
by the company by telephone and by letter dated November 18, 1999. This is the first
public notice issued by the FDA.
The Medi-First Extra Strength
Non-Aspirin Acetaminophen 500 mg, an over-the-counter pain reliever, packaged in 2 tablet
unit dose packets. (NDC #47682-804-99) The recalled product bears lot number 2091 EXP
7/03. Over 448 cartons were distributed in Colorado, California, Texas, Missouri,
Arkansas, Wisconsin, Alabama, Michigan, Indiana, Tennessee, Florida, Georgia, South
Carolina and Illinois.
Questions concerning this recall may
be directed to the FDA at 1-888-INFO-FDA.
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