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SafetyAlerts
September 6, 2001

Nittany Pharmaceuticals, Inc. Recalls Caffeine 200 mg Tablets

Milroy, PA.  (SafetyAlerts) - The Food and Drug Administration (FDA) said today that Nittany Pharmaceuticals, Inc. is recalling Overtime Stimulant tablets Caffeine tablets, 200 mg caffeine, sold in 100 count and 500 count bottles.

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

RECALL NUMBER, PRODUCT AND CODE:
D-271-1 Overtime Stimulant tablets, 200 mg caffeine, sold in 100 count and 500 count bottles. The label states that the product is distributed by BDI Pharmaceuticals, A Division of Body Dynamics Inc., Carmel, IN.

CODES:
Lot 6085 exp. 7/01 and Lot 10362 exp. 2/03.

REASON:
STABILITY: There is no data to support labeled expiry date.

MANUFACTURER/RECALLING FIRM:
Nittany Pharmaceuticals, Inc., Milroy, PA.

RECALLED BY:
Manufacturer, by telephone and letter on 6/27/01.

FIRM INITIATED RECALL:
Ongoing.

DISTRIBUTION:
IN.

QUANTITY:
125 bottles.

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

 
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.