US Drug Recall Register
Class II · Moderate risk Terminated Initiated Aug 8, 2022 (4 years ago)

Corsair Personal Care 99X Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%)128 Fl…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

What was recalled

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

Recalling firm
Midlab Incorporated
Origin
TN, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1464-2022

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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