Saniderm ADVANCED HAND SANITIZER — Class II drug recall D-1412-2020
Terminated recall by POLARIZED LLC, reported 2020-08-05, distributed nationwide. CGMP Deviations: Product was found to be below the label claim for ethanol content and the presence of undecla
| Recall number | D-1412-2020 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | POLARIZED LLC, Lewes, DE, United States |
| Recall initiated | 2020-06-25 |
| Classified | 2020-07-28 |
| Reported by FDA | 2020-08-05 |
| Terminated | 2020-12-02 |
| Distributed | Nationwide (US) |
| Reason classes | undeclared allergen, chemical contamination, labeling, cgmp |
| UPC / GTIN / UDI-DI | 00860003633915 |
Product
Saniderm ADVANCED HAND SANITIZER, 70% Alcohol Content, 1 Liter bottles, Distributed by Polarized, LLC, Produced by Eskbiochem SA de CV, Mexico Japon 50, Celaya, Gto., Mexico, 38010. UPC 8 60003 63391 5.
Reason for recall
CGMP Deviations: Product was found to be below the label claim for ethanol content and the presence of undeclared 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-1412-2020. 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.