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Med Nap Towelettes Recalled Over CGMP Deviations

🟡 MODERATE RISK — CLASS II
Agency: Food and Drug Administration (FDA)  |  Date: 20260311  |  Units: N/A  |  Risk: Class II

This alert was compiled from official government recall data published by the FDA using automated analysis. All facts are sourced directly from official records. Last verified April 6, 2026.

Med Nap BZK Antiseptic Towelettes (Benzalkonium Chloride 0.13%), 100 Towelettes, Manufactured by: Acme United Corporation, 1 Waterview Dr, Shelton, CT 06481, NDC 0924-0246-01. recalled by ACME UNITED CORPORATION - CGMP Deviations

Stock photo for illustration — not the actual recalled product. Photo by Kelly Sikkema on Unsplash

Did you recently purchase Med Nap BZK Antiseptic Towelettes? If so, you’ll want to read this. A new product recall in the United States has been issued for these towelettes due to CGMP deviations. It's important for American shoppers to check if their product is affected.

Med Nap BZK Antiseptic Towelette Recall: What You Need to Know

Acme United Corporation is recalling their Med Nap BZK Antiseptic Towelettes (Benzalkonium Chloride 0.13%), 100 Towelettes. The product, manufactured by Acme United Corporation located in Shelton, CT, and bearing NDC 0924-0246-01, is being recalled nationwide. This means if you purchased it anywhere in the U.S., from California to New York, you could be affected. You might have purchased this item at local pharmacies or even from larger retailers.

Background of the Issue

Before we dive into the specifics, let’s clarify what CGMP deviations are. CGMP stands for Current Good Manufacturing Practice regulations enforced by the FDA. These regulations ensure that drug products are consistently produced and controlled according to quality standards. A deviation means that the manufacturing process didn't fully comply with these standards, which can potentially impact the safety and efficacy of the product.

What's the Hazard?

The reason for this product recall in the United States is CGMP deviations in the manufacturing process. While the FDA has classified this as a Class II recall, it means there is a potential for a temporary or medically reversible adverse health consequence or where the probability of serious adverse health consequences is remote. Nobody wants to find out their antiseptic towelettes, meant to protect them, aren't manufactured up to standard. The agency confirmed that these deviations raise concerns about the quality and sterility of the towelettes, potentially leading to ineffective sanitation and increased risk of infection.

Which Products are Affected?

Here are the specific lot numbers and expiration dates for the affected Med Nap BZK Antiseptic Towelettes. Checking these numbers is crucial for U.S. consumers. To find this information, check the packaging of your towelettes. If you flip the container over, you'll find the lot number and expiration date printed on the label. Here's the list:

  • Lot #: MN09322, Exp. Date Mar 2027
  • Lot #: MN15222, Exp. Date May 2027
  • Lot #: MN21622, Exp. Date Jul 2027
  • Lot #: MN31822, Exp. Date Oct 2027
  • Lot #: MN06223, Exp. Date Feb 2028
  • Lot #: MN06323, Exp. Date Feb 2028
  • Lot #: MN12523, Exp. Date Apr 2028
  • Lot #: MN16123, Exp. Date May 2028
  • Lot #: MN20523, Exp. Date Jun 2028
  • Lot #: MN20623, Exp. Date Jun 2028
  • Lot #: MN20723, Exp. Date Jun 2028
  • Lot #: MN23223, Exp. Date Jul 2028
  • Lot #: MN31123, Exp. Date Oct 2028
  • Lot #: MN300524, Exp. Date Dec 2028
  • Lot #: MN300624, Exp. Date Dec 2028
  • Lot #: MN302624, Exp. Date Dec 2028
  • Lot #: MN302724, Exp. Date Dec 2028
  • Lot #: MN303324, Exp. Date Dec 2028

What To Do If You Have Recalled Towelettes

If you have purchased any of the Med Nap BZK Antiseptic Towelettes with the above lot numbers, here’s what you should do right now:

  1. Stop using the product immediately to avoid any potential health risks.
  2. Contact your healthcare provider if you have experienced any adverse health effects from using the towelettes. Tell them you used a batch of antiseptic towelettes that are part of a nationwide recall.
  3. Dispose of the product safely, following local regulations for discarding potentially compromised medical supplies.
  4. Contact Acme United Corporation for more information and possible reimbursement options; their contact information should be available on their website.

A Note About Acme United Recalls

While every recall situation is different, it's worth noting that Acme United has had other recalls in the past. This doesn't necessarily indicate a pattern of negligence, but it does highlight the importance of ongoing vigilance in manufacturing processes. Keep an eye out for future announcements from the company or the FDA.

Frequently Asked Questions

Q: What does "CGMP Deviations" mean?

CGMP Deviations refer to failures to adhere to the Current Good Manufacturing Practice regulations set by the FDA. These regulations ensure that products are consistently produced and controlled according to quality standards.

Q: How serious is a Class II recall?

A Class II recall means that the product may cause temporary or medically reversible adverse health consequences or that the probability of serious adverse health consequences is remote.

Q: Where were these towelettes sold?

These towelettes were distributed nationwide within the United States, so if you live anywhere in the U.S. and purchased this product, it could potentially be affected.

Q: What if I already used the towelettes?

Monitor yourself for any signs of infection or adverse reactions, and contact your healthcare provider if you have any concerns. Be sure to inform them about the recall.

Q: How many recalls does the FDA issue per year?

The number of recalls issued by the FDA varies, but they typically issue hundreds of recalls each year across various product categories, from food to medical devices.

This recall was announced by the U.S. Food and Drug Administration (FDA). For the official notice and complete details, visit www.fda.gov.

⚠️ If You Own This Product:
Stop using it right away and follow the steps above. You may be entitled to a full refund, free repair, or replacement at no cost.
This article is based on official recall data from the Food and Drug Administration (FDA). Last verified on April 6, 2026.
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