PlainRecalls
FDA Drug Moderate Class II Terminated

Maxim Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%) packaged in a) 1 U.S. Gallon (3.78 Liters) drums UPC 7 61841 02502 6 and b) 55 U.S. Gallon drums (208 Liters) UPC 0 07 61841 02504 0, Midlab 140 Private Brand Way, Athens, TN 37303

Reported: August 31, 2022 Initiated: August 8, 2022 #D-1463-2022

Product Description

Maxim Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%) packaged in a) 1 U.S. Gallon (3.78 Liters) drums UPC 7 61841 02502 6 and b) 55 U.S. Gallon drums (208 Liters) UPC 0 07 61841 02504 0, Midlab 140 Private Brand Way, Athens, TN 37303

Reason for Recall

CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride.

Details

Recalling Firm
Midlab Incorporated
Units Affected
892 gallons and one 55-gallon drum
Distribution
Naionwide within the United States
Location
Athens, TN

Frequently Asked Questions

What product was recalled?
Maxim Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%) packaged in a) 1 U.S. Gallon (3.78 Liters) drums UPC 7 61841 02502 6 and b) 55 U.S. Gallon drums (208 Liters) UPC 0 07 61841 02504 0, Midlab 140 Private Brand Way, Athens, TN 37303. Recalled by Midlab Incorporated. Units affected: 892 gallons and one 55-gallon drum.
Why was this product recalled?
CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride.
Which agency issued this recall?
This recall was issued by the FDA Drug on August 31, 2022. Severity: Moderate. Recall number: D-1463-2022.