FDA Recall D-0363-2026

ACME UNITED CORPORATION · Shelton, CT

Class II Ongoing 114 days on record

Moderate impact — Class II recall — temporary or medically reversible adverse health consequence possible; remote probability of serious adverse health consequence.

Product

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

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

Quantity: N/A

Reason for recall

CGMP Deviations

Recall record

Recall number: D-0363-2026
Classification: Class II
Status: Ongoing
Voluntary or mandated: Voluntary: Firm initiated
Firm notification: Letter
Distribution: Nationwide within the United States
Recall initiated: 2026-01-20
Classified by FDA Center: 2026-03-02
FDA published: 2026-03-11
Recalling firm: ACME UNITED CORPORATION
Firm location: Shelton, CT

Operational response

Class II recalls indicate possible temporary or reversible health consequences. Remove affected lots from active dispensing. Segregate inventory. Check the firm’s recall notification for guidance on patient outreach.

For the official FDA enforcement record, see FDA's Recall Search.

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