November 30, 1999SSS/Pfeiffer Pharmaceuticals
Koleprin DM Caplets Recalled
Atlanta, GA (SafetyAlerts) - The Food and Drug
Administration (FDA) today reported that SSS/Pfeiffer Pharmaceuticals is recalling
Koleprin DM Caplets, cough and cold medication in 30 caplet bottles, because of friability
failure at 3 month stability.
This ongoing Class III recall was initiated
by the company, June 14, 1999 by letter. This is the first notice the FDA has issued
to the general public of the recall.
Over 2,500 units were distributed
nationwide and bear the lot number and expiration date of #98603 EXP 2/01
Questions concerning this recall may
be directed to the FDA at 1-888-INFO-FDA.
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