ACME United Corporation recalls Medi-First Antiseptic Wipes with CGMP deviations. Check NDC 47682-122-33 and lot numbers for affected items.
CGMP Deviations
ACME United Corporation is recalling Medi-First Antiseptic Wipes due to CGMP deviations. This means the product may not meet quality standards, but the recall does not specify a specific hazard or risk to consumers.
CGMP deviations refer to failures in the manufacturing process that could affect product quality. This may mean the antiseptic wipes do not meet the required standards for safety and effectiveness, but the recall does not specify a specific hazard or risk to consumers.
Anyone who owns or uses Medi-First Antiseptic Wipes with the specified lot numbers and NDC code. People using these wipes for medical purposes may be at risk if the product does not meet quality standards.
Check the product label for NDC 47682-122-33 and lot numbers MN15922 (exp. Apr 2027), MN31022 (exp. Oct 2027), or MN27223 (exp. Aug 2028).
Look for NDC 47682-122-33 and lot numbers MN15922, MN31022, or MN27223 on the box.
The recall is due to CGMP deviations, which means the product may not meet quality standards, but the specific hazard is not described in the notice.
The recall does not specify a remedy, so check the product label for the NDC and lot numbers to determine if it is affected.
The recall does not specify a specific hazard or risk to health, so there is no known risk to consumers.
We’ve drafted a message you can send ACME UNITED CORPORATION to request your refund or repair — edit it as you like.
Subject: Recall D-0365-2026 — ACME UNITED CORPORATION ACME UNITED CORPORATION Hello, I own a ACME UNITED CORPORATION that is covered by recall D-0365-2026 from ACME UNITED CORPORATION. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.