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January 27, 2000

Vitalabs, Inc. Recalls "Mega Min" Dietary Supplement

Jonesboro, GA (SafetyAlerts) - The Food and Drug Administration (FDA) today reported that Vitalabs, Inc. is recalling Mega Min Dietary Supplement because some bottles labeled as "Mega Min" actually contain a different supplement, namely, "Formula 7".

The recalled product, an over-the-counter dietary supplement was sold in 100-tablet bottles and can be identified by the lot number of 019-3061.

According to FDA, 2-3 cases (48-72 bottles) were distributed in the Southeastern United States.

This Class III recall was initiated by Vitalabs by letter August 30, 1999.  This is the first public notice issued by the FDA.  The FDA considers this recall to be complete.

Questions concerning this recall may be directed to the FDA at 1-888-INFO-FDA.
FDA Recall #f-088-0

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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