Corsair Personal Care 99X Instant Foam Hand Sanitizer — Class II drug recall D-1464-2022
Terminated recall by Midlab Incorporated, reported 2022-08-31. CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride.
| Recall number | D-1464-2022 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Midlab Incorporated, Athens, TN, United States |
| Recall initiated | 2022-08-08 |
| Classified | 2022-08-25 |
| Reported by FDA | 2022-08-31 |
| Terminated | 2023-08-15 |
| Reason classes | cgmp |
| Lot numbers | 06172022-1 |
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 for recall
CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1464-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.