FDA Drug Recalls

Recalls / Class II

Class IID-0363-2026

Product

Max Packaging Antibacterial Towelette (Benzalkonium Chloride 0.13%), 1 towelette, 4x7, Max Packaging, Made in the USA, NDC 59647-750-01

Affected lot / code info
Lot #: MN24523, Exp. Date July 2028; MN27123, Exp. Date Aug 2028; MN28223, Exp. Date Sep 2028.

Why it was recalled

CGMP Deviations

Recalling firm

Firm
ACME UNITED CORPORATION
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
1 Waterview Dr Ste 200, N/A, Shelton, Connecticut 06484-4368

Distribution

Quantity
N/A
Distribution pattern
Nationwide within the United States

Timeline

Recall initiated
2026-01-20
FDA classified
2026-03-02
Posted by FDA
2026-03-11
Status
Ongoing

Source: openFDA Drug Enforcement endpoint. Recall record D-0363-2026. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.