Florance Morris ANTISEPTIC Hand Sanitizer — Class II drug recall D-0796-2021
Terminated recall by Grupo Asimex de Mexico SA de CV, reported 2021-09-22, distributed nationwide. CGMP Deviations: All other lots are being recalled because they were manufactured under the same conditions as
| Recall number | D-0796-2021 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Grupo Asimex de Mexico SA de CV, Ciudad De Mexico, N/A, Mexico |
| Recall initiated | 2020-08-14 |
| Classified | 2021-09-13 |
| Reported by FDA | 2021-09-22 |
| Terminated | 2023-10-17 |
| Distributed | Nationwide (US) |
| Reason classes | chemical contamination, cgmp |
Product
Florance Morris ANTISEPTIC Hand Sanitizer (ethyl alcohol 70%), packaged in a) 8.45 fl oz (250 mL) bottles and b) 33.81 fl oz (1L) bottles, Distributed by: Asimex International LLC, 9100 S Dadeland Blvd, Ste 912, Miami, FL 33156, COUNTRY OF ORIGIN: MEXICO.
Reason for recall
CGMP Deviations: All other lots are being recalled because they were manufactured under the same conditions as the product lots found to contain methanol.
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-0796-2021. 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.