Max Packaging recalls antibacterial towelettes with benzalkonium chloride due to CGMP deviations. Affected lots expire July-September 2028. No specific remedy stated in official notice.
CGMP Deviations
Max Packaging is recalling antibacterial towelettes that were made with benzalkonium chloride due to manufacturing deviations. This recall affects specific lots that expire between July and September 2028. The product was made in the USA and sold under the brand Max Packaging.
The product was made with benzalkonium chloride due to CGMP deviations, which are regulatory violations in manufacturing processes. These deviations could lead to potential safety issues with the product's quality and safety.
Owners of Max Packaging antibacterial towelettes with the specific lot numbers listed in the recall notice are affected. People using these towelettes for personal hygiene are most at risk.
Check the lot number on the towelette packaging, which should be MN24523 (expires July 2028), MN27123 (expires August 2028), or MN28223 (expires September 2028). The product is a 1 towelette, 4x7 size made in the USA.
Look for lot numbers MN24523, MN27123, or MN28223 on the towelette packaging.
The official recall notice does not state whether the product is safe to use. The product was recalled due to CGMP deviations, but no specific safety concerns were detailed.
The official recall notice does not specify any remedy or action steps for affected products.
The product was made in the USA, with specific expiration dates of July 2028, August 2028, and September 2028.
We’ve drafted a message you can send Max Packaging to request your refund or repair — edit it as you like.
Subject: Recall D-0363-2026 — Max Packaging Max Packaging Hello, I own a Max Packaging that is covered by recall D-0363-2026 from Max Packaging. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
