HIGHFDA DRUG

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.

Official notice

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DRUG
Recall date
January 20, 2026
Status
ACTIVE
Severity
7/10

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

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
MED NAP CLEANSING TOWELETTE, ACME UNITED CORPORATION
Product type
Cleansing Towelettes with Benzalkonium Chloride
Model numbers
MN15923, MN25822
UPC codes
0924-0243, 0924-0243-00, 0924-0243-01
Sizes
5"x7"
Sold at
Multiple Retailers
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    January 20, 2026

  2. Reported by FDA DRUG

    March 11, 2026

  3. RecallRadar source check

    March 18, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

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

About This Product

Med Nap Cleansing Towelettes are used for surface or skin cleansing with benzalkonium chloride as an antiseptic active ingredient. The 5"x7" wipes come in bulk packaging for healthcare or facility use.

Why This Is Dangerous

CGMP deviations suggest potential quality-control issues in manufacturing. This could affect product consistency or safety, though no injuries are reported yet.

Industry Context

This recall is not described as part of a broader CGMP-deviations trend in the industry.

Real-World Impact

The recall affects nationwide distribution. Consumers should stop using the product to avoid potential quality concerns and await guidance on refunds or replacements.

Practical Guidance

How to identify if yours is affected

  1. Check lot MN15923 or MN25822 on the package
  2. Verify Expiration May 2028 or Aug 2027
  3. Look for NDC 0924-0243-00 and size 5"x7"
  4. Confirm it was manufactured in Brooksville, FL

Where to find product info

Label on packaging and FDA recall page (D-0370-2026)

What timeline to expect

Refunds or replacements expected within 4-6 weeks after confirmation of eligibility

If the manufacturer is unresponsive

  • Escalate with the recall page and company contacts
  • File a consumer complaint with the CPSC if needed
  • Consult your healthcare provider for guidance if exposure occurred

How to prevent similar issues

  • Buy from reputable retailers; verify NDC 0924-0243-00 before purchase
  • Avoid bulk medical wipes with unknown lot numbers
  • Monitor recall updates and register for recall notices

Documentation advice

Keep product packaging, recall letter, purchase receipts, and all correspondence with the company

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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.

Key Facts

  • CGMP Deviations cited as the recall reason
  • 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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