HIGH

Acme United MED NAP BZK Antiseptic Towelettes Recalled in 2026 (100-Count)

Acme United Corporation recalled Med Nap BZK Antiseptic Towelettes, 100-count, distributed nationwide. The FDA-listed CGMP deviations raise concerns about manufacturing quality and product safety. Consumers and healthcare providers should stop using the product and follow the recall letter for guidance.

Quick Facts at a Glance

Recall Date
January 20, 2026
Hazard Level
HIGH
Brands
Acme United Corporation, Med Nap Benzalkonium Chloride Antiseptic
Category
Health & Personal Care
Sold At
Unknown
Geographic Scope
1 states
At-Risk Groups
GENERAL, PREGNANT

Hazard Information

CGMP Deviations

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact ACME UNITED CORPORATION or your healthcare provider for guidance. Notification method: Letter

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About This Product

Med Nap BZK Antiseptic Towelettes are consumer medical supplies used to clean and disinfect skin surfaces. They are sold as 100-count packages for clinical and home use.

Why This Is Dangerous

CGMP deviations indicate potential quality issues in manufacturing that could affect product safety or efficacy. The exact impact on the wipes is not detailed in the notice.

Industry Context

This recall is not described as part of a broader industry pattern.

Real-World Impact

The recall may reduce access to antiseptic supplies for consumers and healthcare settings until replacement products are available. No injuries reported.

Practical Guidance

How to identify if yours is affected

  1. Check for lot MN09322, MN15222, MN21622, MN31822, MN06223, MN06323, MN12523, MN16123, MN20523, MN20623, MN20723, MN23223
  2. Verify expiration dates ranging Mar 2027 to Jun 2028 where shown
  3. Look for the Med Nap BZK antiseptic towellettes packaging that states 0.13% benzalkonium chloride and 100-count package

Where to find product info

FDA recall page for D-0366-2026 and the Acme United recall notice

What timeline to expect

The recall notice does not specify replacement timelines. Consumers should await guidance from Acme United Corporation.

If the manufacturer is unresponsive

  • File a complaint with the FDA Consumer Product Safety Commission if the company is unresponsive
  • Keep copies of the recall letter and your communications
  • Record the lot numbers and dates of purchase if known

How to prevent similar issues

  • Always verify CGMP-compliant manufacturing in healthcare products
  • Check for current recalls before consuming or using antiseptic products
  • Prefer products with clear batch/lot information and expiry dates on packaging

Documentation advice

Keep the recall letter, photos of packaging, purchase receipts, and any correspondence with the manufacturer for records

Product Details

Brand: Med Nap Benzalkonium Chloride Antiseptic; Product: BZK Antiseptic Towelettes, 0.13% Benzalkonium Chloride, 100-count; Manufacturer: Acme United Corporation, 1 Waterview Dr, Shelton, CT 06481; Model numbers and lot details: MN09322 (Lot MN09322, Exp Mar 2027); MN15222 (Exp May 2027); MN21622 (Exp Jul 2027); MN31822 (Exp Oct 2027); MN06223; MN06323 (Exp Feb 2028); MN12523 (Exp Apr 2028); MN16123 (Exp May 2028); MN20523; MN20623; MN20723 (Exp Jun 2028); MN23223; Pack size: 100-towelette count; Distribution: Nationwide in the United States

Key Facts

  • 100-count package
  • CGMP deviations cited by FDA enforcement listing
  • Lot numbers MN09322, MN15222, MN21622, MN31822, MN06223, MN06323, MN12523, MN16123, MN20523, MN20623
  • MN20723, MN23223; Expiration dates range Mar 2027 to Jun 2028
  • Nationwide distribution in the United States
  • No injuries or deaths reported to date

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
6/ 10
Affected Groups
GENERALPREGNANT
Injury Types
POISONINGELECTRICALLACERATIONBURNSUFFOCATIONOTHER

Product Details

Model Numbers
MN09322
MN15222
MN21622
MN31822
MN06223
+7 more
UPC Codes
0924-0246
0924-0246-00
0924-0246-01
+2 more
Affected States
ALL
Report Date
March 11, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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