Dynarex — Class II drug recall D-0375-2026
Ongoing recall by ACME UNITED CORPORATION, reported 2026-03-11, distributed nationwide. CGMP Deviations
| Recall number | D-0375-2026 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | ACME UNITED CORPORATION, Shelton, CT, United States |
| Recall initiated | 2026-01-20 |
| Classified | 2026-03-02 |
| Reported by FDA | 2026-03-11 |
| Distributed | Nationwide (US) |
| Reason classes | cgmp |
| NDC | 67777-0245, 67777-0245-01, 67777-0245-02, 67777-0245-04, 67777-0245-05, 67777-0245-06, 67777-0245-07, 67777-0245-08, 67777-0245-11, 67777-0245-14, 67777-0245-15, 67777-0245-16, 67777-0245-17, 67777-0245-18 |
| Lot numbers | 52347-R, 52348-R, 52349-R, 52350, 52351-R, 52352, 53518 |
| Expiration dates | 2027-03-20, 2027-06-20 |
Product
Dynarex, BZK Antiseptic Towelettes (Benzalkonium Chloride 0.13%), 100 packets, 5x7, Manufactured for Dynarex Corporation, 10 Glenshaw Street, Orangeburg, NY 10962,USA, NDC 67777-245-01
Reason for recall
CGMP Deviations
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-0375-2026. 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.