November 30, 1999Mikart, Inc. Duratuss G Tablets
Atlanta, GA (SafetyAlerts) - The Food and Drug
Administration (FDA) today reported that Mikart, Inc. is recalling Duratuss G Tablets
because of dissolution failure.
This ongoing Class III recall was initiated
by the company, June 22, 1999 by telephone. This is the first notice the FDA has
issued to the general public of the recall.
The recalled tablets were distributed
in Wisconsin and bear the lot numbers of J980726A or J9800727A.
Questions concerning this recall may
be directed to the FDA at 1-888-INFO-FDA.
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