ACME UNITED recalled Max Packaging Antibacterial Towelette nationwide in the United States after CGMP deviations were identified. Manufacturing quality deviations prompted the recall, classified as Class II and labeled as high hazard. Stop using the product immediately and contact ACME UNITED CORPORATION or your healthcare provider for guidance.
CGMP Deviations
Consumers and healthcare providers should stop using this product immediately. Contact ACME UNITED CORPORATION or your healthcare provider for guidance. Notification method: Letter
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Product: Max Packaging Antibacterial Towelette (Benzalkonium Chloride 0.13%). Form: 1 towelette. Pack size: 4x7. NDC: 59647-750-01. Lot numbers: MN24523; MN27123; MN28223. Expiration: MN24523 by July 2028; MN27123 by August 2028; MN28223 by September 2028. Manufactured in the United States. Sold nationwide in the United States. Manufacturer: ACME UNITED CORPORATION.
The recall centers on CGMP deviations in manufacturing. The deviations could affect the quality and consistency of the antibacterial towelettes.
1. Stop using the product immediately. 2. Consult a healthcare provider if you have health concerns. 3. For guidance and next steps, contact ACME UNITED CORPORATION or review the FDA recall page for official instructions.
Recall page and official details: https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=D-0363-2026. No public phone number or consumer helpline is listed in the notice.
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