Midlab Incorporated: Drug Recall

Recall #D-1464-2022 · 08/08/2022

Class II: Risk

Recall Details

Recall Number
D-1464-2022
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

Reason for Recall

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

Product Description

Corsair Personal Care 99X Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%)128 Fl. Oz. (1 Gal.) 3.78 liters bottles, Southern Products & Services, Inc. 2515 Jake Drive Ste B, Cumming, GA 30028

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.