Ohm Hand Sanitizer — Class II drug recall D-0263-2023
Terminated recall by Urban Electric Power, reported 2023-02-15, distributed nationwide. CGMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.
| Recall number | D-0263-2023 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Urban Electric Power, Pearl River, NY, United States |
| Recall initiated | 2023-01-17 |
| Classified | 2023-02-08 |
| Reported by FDA | 2023-02-15 |
| Terminated | 2024-02-26 |
| Distributed | Nationwide (US) |
| Reason classes | cgmp |
Product
Ohm Hand Sanitizer (alcohol (ethanol) 70 % v/v), packaged in a) 2 FL OZ (60 ML), b) 3 FL OZ (88 ML) bottles, c) 10 FL OZ (295 ML) bottles, d)12 FL OZ (355 ML) bottles, e)16 FL OZ (473 ML) bottles, f) 64 FL OZ (1892 ML) bottles, g) 128 FL OZ (3785 ML) bottles
Reason for recall
CGMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.
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-0263-2023. 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.