HIGH

Med Nap Cleansing Towelettes Recall Expanded Over CGMP Deviations (2026)

ACME United Corporation recalls Med Nap Cleansing Towelettes, 5"x7" Benzalkonium Chloride 0.13%, distributed nationwide. CGMP Deviations prompted the recall. Stop using the product now and contact ACME United or a healthcare provider for guidance.

Quick Facts at a Glance

Recall Date
January 20, 2026
Hazard Level
HIGH
Brands
MED NAP CLEANSING TOWELETTE, ACME UNITED CORPORATION
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

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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Product Details

Brand: MED NAP CLEANSING TOWELETTE. Manufacturer: ACME UNITED CORPORATION. Size: 5" x 7". Packaging: 1,000 case/bulk. NDC: 0924-0243-00. Lot numbers: MN15923 and MN25822. Expiration: MN15923 area May 2028; MN25822 area Aug 2027. Sold nationwide in the United States. Made in USA. Recall Date: 2026-01-20. FDA Enforcement Report: D-0370-2026. Status: ACTIVE.

The Hazard

CGMP Deviations underpin the recall. The towelettes use benzalkonium chloride as an active antiseptic. The deviations raise concerns about manufacturing quality and product consistency. Consumers should treat the product as potentially unsafe until more information is available.

Reported Incidents

No specific injuries or adverse events are cited in the recall notice. The agency lists the issue as a quality-control deviation rather than a reported injury.

What to Do

1. Stop using the product. 2. Contact ACME United Corporation or your healthcare provider for guidance. 3. Monitor for recall updates on the FDA enforcement page. 4. Follow instructions for refunds or replacements when issued.

Contact Information

Company: ACME United Corporation. Recall page: FDA enforcement report D-0370-2026. Phone: Unknown. Website: Unknown. Hours: Unknown.

Key Facts

  • CGMP Deviations cited as the recall reason
  • NDC 0924-0243-00
  • Two lots affected: MN15923 (May 2028 exp) and MN25822 (Aug 2027 exp)
  • 1,000-case bulk packaging
  • Distributed nationwide in the United States

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
7/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
MN15923
MN25822
UPC Codes
0924-0243
0924-0243-00
0924-0243-01
Affected States
ALL
Report Date
March 11, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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