August 28, 2002
GOJO Industries Has Recalled GOJO Skin Lotion
- The Food and Drug Administration (FDA)
has released the
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)
LOT NUMBERS: 134239, 138256, 147523, 151914, 152499, 153752, 160436,
GOJO Industries, Inc., Cuyahoga Falls, OH, by fax on July 25, 2002. Firm
initiated recall is ongoing.
Subpotent; active ingredient Allantoin (stability).
VOLUME OF PRODUCT IN COMMERCE