April 17, 2002
GOJO Industries Has Recalled HAND MEDIC
Antiseptic Skin Treatment
Cuyahoga Falls, OH (SafetyAlerts)
- The Food and Drug Administration (FDA) said that GOJO Industries, Inc. has recalled HAND MEDIC
Antiseptic Skin Treatment.
HAND MEDIC Antiseptic Skin Treatment, OTC, packaged in 500 ml cartridges,
and 2 oz, 4 oz, and 8 oz bottles. Active ingredient: Benzalkonium Chloride
0.1%. Recall # D-237-2.
The 500 ml cartridges are sealed poly bags inside a rectangular cardboard
box, 6 per case.
All bottles are black plastic, 12 per case (2 oz & 4 oz bottles), or 6 per
case (8 oz bottles).
The 500 ml cartridges, and the 4 oz and 8 oz bottles are packaged under the
GOJO brand label; and the 2 oz bottles are packaged under either the GOJO
brand or Pro-Link brand labels.
The product catalog numbers are as follows:
#8242-06 (500 ml cartridges); #8142-12 (2 oz); #8147-12 (4 oz).
#8145-06 (8 oz)
Lot Numbers: 165461, 166095, 166581, 166826, 167503,
168453, and 168912.
GOJO Industries, Inc., Cuyahoga Falls, OH, by fax on March 26, 2002.
Firm initiated recall is ongoing.
Superpotency of the active ingredient (Benzalkonium Chloride).
VOLUME OF PRODUCT IN COMMERCE