ACME UNITED CORPORATION recalls Dukal BZK Antiseptic Towelettes due to CGMP deviations. Affected lots have specific expiration dates and manufacturing codes. Consumers should check their product details and contact the manufacturer for instructions.
CGMP Deviations
ACME UNITED CORPORATION has recalled Dukal BZK Antiseptic Towelettes (1000 packs per case) because of CGMP deviations. This means the product may not meet safety standards, though the recall does not specify a risk of injury or harm.
CGMP deviations refer to failures in the manufacturing process that could affect product safety. However, the recall does not specify what the deviations are or how they might impact the product's safety.
Owners of Dukal BZK Antiseptic Towelettes with specific lot numbers and expiration dates listed in the recall are affected. The recall targets consumers who purchased these products from the manufacturer.
Check the product label for the lot numbers: MN31621 (exp. Oct 2026), MN14522 (exp. Apr 2027), and other specific lot codes listed in the recall. The expiration dates range from October 2026 to November 2028.
Look for the lot numbers and expiration dates on the product label to determine if it is affected.
The recall is due to CGMP deviations, which are manufacturing process failures that may affect product safety, though the specific risks are not detailed.
Check the product label for the lot numbers and expiration dates listed in the recall. Contact ACME UNITED CORPORATION for further instructions.
The recall does not specify any risk of injury or harm, so the danger level is unknown.
We’ve drafted a message you can send Dukal to request your refund or repair — edit it as you like.
Subject: Recall D-0360-2026 — Dukal Dukal Hello, I own a Dukal that is covered by recall D-0360-2026 from Dukal. 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.