HIGHFDA DRUG

First Aid Only BZK Antiseptic Towelettes Recalled for CGMP Deviations in 2026 (212,607,900 Units)

ACME United Corporation recalled 212,607,900 First Aid Only BZK Antiseptic Towelettes sold nationwide. The recall cites CGMP deviations in manufacturing. Consumers should stop using the product immediately and contact ACME United Corporation 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
4/10

Quick Facts at a Glance

Recall Date
January 20, 2026
Hazard Level
HIGH
Brands
First Aid Only BZK Antiseptic, 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
First Aid Only BZK Antiseptic, Acme United Corporation
Product type
BZK Antiseptic Towelettes (0.13%)
Model numbers
MN26222, MN34722, MN25922, MN00523
UPC codes
0924-7116, 0924-7116-00, 0924-7116-04, 0924-7116-05, 0924-7116-03, 0924-7116-01, 0924-7116-02
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

    April 13, 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

The product is a benzalkonium chloride–based antiseptic towlette used for wound cleansing and cleaning skin. It comes in boxes of 100 wipes and is sold under the First Aid Only BZK Antiseptic brand.

Why This Is Dangerous

CGMP deviations indicate potential quality-control issues in manufacturing. The recall focuses on manufacturing process concerns rather than an explicit chemical hazard from use.

Industry Context

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

Real-World Impact

Consumers may need to discard affected lots and seek guidance from the company. There is potential inconvenience and cost associated with replacing the product.

Practical Guidance

How to identify if yours is affected

  1. Identify NDC 0924-7116-04 on the packaging.
  2. Check lot numbers MN26222, MN34722, MN25922, MN00523.
  3. Confirm expiration dates November 2027 or December 2027.

Where to find product info

Packaging should display NDC, lot numbers, and expiration date; the FDA recall page provides official details.

What timeline to expect

Refund or replacement timelines typical for recalls are 4-8 weeks, though official timelines may vary by company.

If the manufacturer is unresponsive

  • Document all communications with ACME United and retailers.
  • File a complaint with the CPSC if you encounter delays or lack of resolution.
  • Consider consulting a consumer attorney for serious issues.

How to prevent similar issues

  • When shopping for antiseptic products, verify CGMP compliance and check for recall notices.
  • Inspect packaging for NDC codes and lot numbers before purchase.
  • Buy from reputable retailers and keep receipts for possible recalls.

Documentation advice

Keep product packaging, lot numbers, expiration dates, purchase receipts, and all recall correspondence as part of your records.

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Product Details

Model numbers and identifiers include MN26222, MN34722, MN25922, MN00523. NDC 0924-7116-04. Sold nationwide in the United States. Quantity recalled: 212,607,900 containers. Recall date: 2026-01-20. Manufacturer: Acme United Corporation.

Key Facts

  • Expiration dates Nov 2027 and Dec 2027

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
4/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
MN26222
MN34722
MN25922
MN00523
UPC Codes
0924-7116
0924-7116-00
0924-7116-04
+4 more
Affected States
ALL
Report Date
March 11, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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