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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Max Packaging Antibacterial Towelette is an antiseptic wipe used for cleaning hands and surfaces. It is sold in 4x7 packs with 1 towelette per unit.
CGMP deviations refer to manufacturing process irregularities that can affect product quality. The recall warns of potential safety or efficacy concerns due to these deviations.
This recall is not indicated as part of a broader industry pattern.
No injuries reported to date. Nationwide distribution means consumers across the United States may have the affected product. Consumers should stop use immediately.
FDA recall page and ACME UNITED notices linked in the recall documentation
Not specified in recall notice
Keep packaging, take photos of lot and expiration dates, save recall notice and correspondence, track submission dates for refunds or replacements
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.
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