ACME United Corporation recalls Dynarex Obstetrical Towelettes Cleanser (Benzalkonium Chloride 0.13%) due to CGMP deviations. Product sold in 100-packet packs with specific lot numbers and expiration dates.
CGMP Deviations
ACME United Corporation is recalling Dynarex Obstetrical Towelettes Cleanser because of manufacturing quality control issues. This recall affects products made in the USA with specific lot numbers and expiration dates.
The product was manufactured with CGMP (Current Good Manufacturing Practice) deviations, which means the production process did not meet regulatory standards. This could lead to potential quality issues with the product, though the exact risk is not specified in the recall notice.
Healthcare providers and individuals using obstetrical towelettes for medical purposes are likely affected. Those using the product in clinical settings or at home for medical care may be at risk.
Check for the product name 'Dynarex Obstetrical Towelettes Cleanser', 100 packets, 5" x 7" size. Look for lot numbers 52347-R through 52352-R and 53518, 53519, with an expiration date of March 2027.
Identify the lot numbers and expiration date on the product packaging to confirm if it is part of the recall.
The product was manufactured with CGMP deviations, which means it did not meet regulatory quality standards.
The recall notice does not specify a remedy, so check the product details to see if it is part of the recall.
Yes, lot numbers 52347-R through 52352-R and 53518, 53519 with an expiration date of March 2027 are affected.
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-0369-2026 — ACME UNITED CORPORATION ACME UNITED CORPORATION Hello, I own a ACME UNITED CORPORATION that is covered by recall D-0369-2026 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.
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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.
