Max Packaging Antibacterial Towelette — Class II drug recall D-0363-2026
Ongoing recall by ACME UNITED CORPORATION, reported 2026-03-11, distributed nationwide. CGMP Deviations
| Recall number | D-0363-2026 |
|---|---|
| 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 | 59647-0750-01 |
| Lot numbers | MN24523, MN27123, MN28223 |
| Expiration dates | 2028-07-20, 2028-08-20, 2028-09-20 |
Product
Max Packaging Antibacterial Towelette (Benzalkonium Chloride 0.13%), 1 towelette, 4x7, Max Packaging, Made in the USA, NDC 59647-750-01
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-0363-2026. 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.