FDA Drug Recalls

Recalls / Class II

Class IID-1464-2022

Product

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

Affected lot / code info
Lot #: 06172022-1

Why it was recalled

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

Recalling firm

Firm
Midlab Incorporated
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
140 Private Brand Way, Athens, Tennessee 37303-1401

Distribution

Distribution pattern
Naionwide within the United States

Timeline

Recall initiated
2022-08-08
FDA classified
2022-08-25
Posted by FDA
2022-08-31
Terminated
2023-08-15
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1464-2022. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class II recall: drug · FDA Drug Recalls