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February 14, 2001

FDA First Notice: Daily-Vite Daily Multiple Vitamin Formula Recalled

Carmel, IN (SafetyAlerts) - The Food and Drug Administration (FDA) said today that Pharmaceutical Corporation of America is recalling - or has recalled - its Daily-Vite Daily Multiple Vitamin Formula.  The product was manufactured under conditions whereby it may have been contaminated with beta-lactam antibiotic drug residues from other products repackaged at the same facility.

This is the first public notice of this Class II recall issued by FDA.

Daily-Vite Daily Multiple Vitamin Formula.

Recall #F-206-1.

All lots on the market at the time the recall was initiated.

Pharmaceutical Corporation of America, Carmel, IN.

Manufacturer, by letter on March 13, 2000. Firm-initiated recall *complete.

*Completed recall: While the FDA has completed processing of this particular recall, it does not necessarily mean this particular product has been fully accounted for.

United States.


Questions concerning this recall may be directed to the FDA at 1-888-INFO-FDA.

Notice of this product warning was sent via email to SafetyAlerts subscribers February 14, 2001.  For more information regarding the SafetyAlerts free email alert service please click here.

Selected Recent Recalls

Health Professional:

Did you know?
During 2000 there were over
1050 products recalled in the United
States for safety reasons!

How many did you hear about?

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The information contained herein has been obtained from sources that the Company believes to be reliable, however, the Company has not independently verified or confirmed the information and the recipient acknowledges that no representations or warranties are being made in connection with the use of the information.