Synergy Hand Sanitizer — Class II drug recall D-1537-2022
Terminated recall by SUPERIOR GLOVE WORKS, LTD., reported 2022-09-21, distributed nationwide. CGMP Deviations: FDA analysis found product to contain acetaldehyde impurity and the Sum of All Impurities, ab
| Recall number | D-1537-2022 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | SUPERIOR GLOVE WORKS, LTD., Acton, Canada |
| Recall initiated | 2022-09-01 |
| Classified | 2022-09-15 |
| Reported by FDA | 2022-09-21 |
| Terminated | 2023-06-27 |
| Distributed | Nationwide (US) |
| Quantity | 7,296 bottles |
| Reason classes | cgmp, specification failure |
| UPC / GTIN / UDI-DI | 00779406201594 |
| Lot numbers | 200513TA |
| Expiration dates | 2023-05 |
Product
Synergy Hand Sanitizer, Non-Sterile Solution to help reduce bacteria that can potentially cause disease, For use when soap and water are not available, Alcohol 80% Topical Solution, Antiseptic, 8.5 oz./ 250 mL bottles, Made and Distributed by: Superior Glove Works Ltd., 36 Vimy Street, Acton, Ontario, L7J 1S1, Canada, Made in Canada, UPC: 779406201594.
Reason for recall
CGMP Deviations: FDA analysis found product to contain acetaldehyde impurity and the Sum of All Impurities, 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-1537-2022. 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.