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SafetyAlerts
June 21, 2001

LotriminÆ AF Spray Liquid Recalled

Cleveland, TN (SafetyAlerts) - The Food and Drug Administration (FDA) said today that Schering-Plough HealthCare Products has recalled certain LotriminÆ AF Spray Liquid because it is misbranded; Lotrimin AF Liquid Spray was incorrectly labeled as Lotrimin AF Deodorant Powder.

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

PRODUCT
LotriminÆ AF Spray Liquid, 4 oz. (113 gram) Aerosol can, The product is an OTC, topically applied antifungal aerosol. The active ingredient is 2% Miconazole Nitrate.

Recall # D-221-1.

CODES:
Lot Number 1A05CC. 1A05CCC Exp 01 04.

MANUFACTURER:
CCL Custom Manufacturing, Inc. Cumberland, RI.

RECALLED BY:
Schering-Plough HealthCare Products, Cleveland, TN., by letter dated May 22, 2001. Firm-initiated recall ongoing.

DISTRIBUTION:
Nationwide.

QUANTITY:
96,500 units (individual cans).

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 June 21, 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.