ACME United Corporation recalls Wipes Plus hand sanitizing wipes due to CGMP deviations. Affected lots have specific expiration dates and manufacturing codes. Consumers should check their product details to determine if they are affected.
CGMP Deviations
ACME United Corporation is recalling Wipes Plus hand sanitizing wipes that were manufactured with CGMP deviations. This recall is due to potential quality issues that could affect product safety.
CGMP deviations refer to failures in the manufacturing process that could lead to product quality issues. These deviations may result in the wipes not meeting safety standards, potentially causing harm if used improperly.
People who own or use Wipes Plus hand sanitizing wipes with the specific lot numbers and expiration dates listed in the recall notice are affected. Those who use these wipes for hand sanitizing are most at risk.
Check the product label for the lot numbers: MN16022 (exp. Aug 2027), MN33922 (exp. Apr 2027), MN31222 (exp. Apr 2027), MN16522 (exp. Oct 2027), MN17022 (exp. Apr 2027), or MN03323 (exp. Jan 2028). The product also has an expiration date and is manufactured by ACME United Corporation.
Look for the lot numbers listed in the recall notice: MN16022, MN33922, MN31222, MN16522, MN17022, or MN03323.
The product was recalled due to CGMP deviations, which are manufacturing process failures that could affect product safety.
Check the product label for the lot numbers listed in the recall notice to determine if you have an affected product.
The recall is due to potential quality issues from manufacturing deviations, but specific safety risks are not detailed in the official notice.
We’ve drafted a message you can send ACME to request your refund or repair — edit it as you like.
Subject: Recall D-0368-2026 — ACME ACME Hello, I own a ACME that is covered by recall D-0368-2026 from ACME. 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.
