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
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.
Lot 6085 exp. 7/01 and Lot 10362 exp. 2/03.
STABILITY: There is no data to support labeled expiry date.
Nittany Pharmaceuticals, Inc., Milroy, PA.
Manufacturer, by telephone and letter on 6/27/01.
FIRM INITIATED RECALL:
Questions concerning this recall may be directed
to the FDA at 1-888-INFO-FDA.