Midlab Incorporated: Drug Recall

Recall #D-1463-2022 · 08/08/2022

Class II: Risk

Recall Details

Recall Number
D-1463-2022
Classification
Class II
Product Type
Drug
Recalling Firm
Midlab Incorporated
Status
Terminated
Date Initiated
08/08/2022
Location
Athens, TN, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
892 gallons and one 55-gallon drum

Reason for Recall

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

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

Distribution Pattern

Naionwide within the United States

Other Recalls by Midlab Incorporated

View all recalls by Midlab Incorporated →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.