Sting Relief Swabs — Class II drug recall D-0122-2026
Ongoing recall by ACME UNITED CORPORATION, reported 2025-11-05, distributed nationwide. Product Mix-up
| Recall number | D-0122-2026 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | ACME UNITED CORPORATION, Shelton, CT, United States |
| Recall initiated | 2025-09-23 |
| Classified | 2025-10-28 |
| Reported by FDA | 2025-11-05 |
| Distributed | Nationwide (US) |
| Quantity | 2,338 boxes |
| UPC / GTIN / UDI-DI | 00738743190015 |
| Lot numbers | 2251994 |
| Model numbers | 19-001 |
| Expiration dates | 2029-09-30 |
Product
Sting Relief Swabs, First Aid Only, 10 Swabs per box, part number 19-001, Manufactured for: Acme United Corporation, 1 Waterview Dr. Shelton, CT, Made in the USA UPC 738743190015
Reason for recall
Product Mix-up
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-0122-2026. 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.