FDA Drug recall D-1464-2022
Corsair Personal Care 99X Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%)128 Fl. Oz. (1 Gal.) 3.78 liters bottles, Southern Produc…
- FDA Drug
- Class II
- terminated
- Published 2022-08-31
On 2022-08-31 the FDA classified a Class II recall of Corsair Personal Care 99X Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%)128 Fl. Oz. (1 Gal.) 3.78 liters bottles, Southern Produc… by Midlab, citing CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1464-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-08-08 |
| Published | 2022-08-31 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Midlab |
| Distribution | n/a |
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
Reason
CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride.
Identifiers
| code_info | Lot #: 06172022-1 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1464-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.