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SafetyAlerts
September 27,2002

Recall Update: Tend Skin International Recall Complete

(SafetyAlerts) - The Food and Drug Administration (FDA) has released the following information.

PRODUCT
a) Tend Skin Lotion (acetylsalicylic acid) 9.7%, 4 oz. (118 mL), 8 oz.
(236 mL) and 16 oz. (472 mL) bottles. Recall # D-403-2;
b) Soft Cell Topical Solution (acetylsalicylic acid) 4 oz bottles.
Recall # D-404-2;
c) Bump No More Topical Solution (acetylsalicylic acid) 9.7%, 4 oz.
(118 mL) and 16 oz. (472 mL) bottles. Recall # D-405-2;
d) Hard Top Intrinsic Nail Hardener Liquid (acetylsalicylic acid)
1/2 ounce. Recall # D-406-2;
e) PUREFECTION Topical Solid (acetylsalicylic acid) Net Wt
2.1 oz. bottle. Recall # D-407-2.

CODE
All lot numbers are included in the recall.

RECALLING FIRM/MANUFACTURER
Recalling Firm: Tend Skin International, Inc., dba The Tend Skin Company, Davie, FL,
by telephone January 8, 2002. Firm initiated recall is complete.

REASON
Failure to comply with Over The Counter monographs (unapproved drug
claims).

VOLUME OF PRODUCT IN COMMERCE
478,873.

DISTRIBUTION
Nationwide.

 
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.