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SafetyAlerts
August 28, 2002

GOJO Industries Has Recalled GOJO Skin Lotion

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

PRODUCT
GOJO Skin Lotion Medicated (Allantoin 0.7%),
5 fl oz tubes NET 148 mL. Recall # D-388-2.

The catalog numbers and packaging configuration are as follows:
#8140-24 (case of 24); #8140-24-B5P00 (case of 24);
#8140-06-BH200 (case of 6); #8140-12-BYR00 (case of 12)

CODE
LOT NUMBERS: 134239, 138256, 147523, 151914, 152499, 153752, 160436,
169565, 170833.

RECALLING FIRM/MANUFACTURER
GOJO Industries, Inc., Cuyahoga Falls, OH, by fax on July 25, 2002. Firm
initiated recall is ongoing.

REASON
Subpotent; active ingredient Allantoin (stability).

VOLUME OF PRODUCT IN COMMERCE
12,719 cases.

DISTRIBUTION
Nationwide.

 
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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.