January 27, 2000Vitalabs, 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
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