Maxim Instant Foam Hand Sanitizer — Class II drug recall D-1463-2022
Terminated recall by Midlab Incorporated, reported 2022-08-31. CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride.
| Recall number | D-1463-2022 |
|---|---|
| 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 |
| UPC / GTIN / UDI-DI | 00761841025026 |
Product
Maxim Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%) packaged in a) 1 U.S. Gallon (3.78 Liters) drums UPC 7 61841 02502 6 and b) 55 U.S. Gallon drums (208 Liters) UPC 0 07 61841 02504 0, Midlab 140 Private Brand Way, Athens, TN 37303
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-1463-2022. 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.