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April 12, 2001

MGP Multi-Vita Drops with Fluoride Recalled

Morton Grove, IL (SafetyAlerts) - The Food and Drug Administration (FDA) said today that Morton Grove Pharmaceuticals, Inc. has recalled certain MGP Multi-Vita Drops with Fluoride because of subpotency prior to expiration date; vitamin C (ascorbic acid.)

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

a) MGP Multi-Vita Drops with Fluoride 0.25 mg., product code 8659, NDC 60432-659-50. Recalled #-158-1.

b) MGP Multi-Vita Drops with Fluoride 0.5 mg., product code 8496, NDC 60432-496-50. Recall #D-159-1.

Product Code 8659, lots 22647A, 22431A, 22657A, 22534A, 22534C, 22534E, 22884-A, 22998A, 23077A, 23184A, 23232A, 23351A;

Product code 8496, lots 22308A, 22460A, 22602A, 22602C, 22769A, 23000A, 23000C, 23032A.

Morton Grove Pharmaceuticals, Inc., Morton Grove, IL.

Manufacturer, by letters dated 3/14/01. Firm-initiated recall ongoing.


434378 – 0.25 mg. Fluoride bottles, 53323 – 0.5 mg. Fluoride bottles.

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 April 12, 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!

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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.