blumen ADVANCED HAND SANITIZER — Class II drug recall D-0023-2021
Terminated recall by 4e Brands North America, Llc, reported 2020-10-07, distributed nationwide. CGMP Deviations: recalled because it was manufactured in the same facility as the product found to contain met
| Recall number | D-0023-2021 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | 4e Brands North America, Llc, San Antonio, TX, United States |
| Recall initiated | 2020-07-11 |
| Classified | 2020-10-07 |
| Reported by FDA | 2020-10-07 |
| Terminated | 2024-02-26 |
| Distributed | Nationwide (US) |
| Quantity | 17,359,247 bottles |
| Reason classes | chemical contamination, cgmp |
| UPC / GTIN / UDI-DI | 00814266023594, 00814266023624, 00814266023693 |
Product
blumen ADVANCED HAND SANITIZER, 70% ALCOHOL CONTENT, (70% ethyl alcohol), packaged as a) 3.4 fl oz / 100 ml bottle, UPC 8 14266 02359 4 b) 7.5 fl. oz./221 ml bottle, UPC 8 14266 02362 4 b) 33.8 fl. oz./1L bottle, UPC 8 14266 02369 3, Distributed in USA and Canada By: 4e Brands Northamerica LLC, 17806 IH-10W, Suite 300, San Antonio, Texas, 78257, Made in Mexico.
Reason for recall
CGMP Deviations: recalled because it was manufactured in the same facility as the product found to contain methanol which represents poor Current Good Manufacturing Practices.
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-0023-2021. 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.