HIGHFDA DRUG

ACME United's First Aid Only BZK Towelettes Recall 2026: CGMP Deviations Prompt Nationwide Action

ACME United Corporation recalled First Aid Only BZK Antiseptic Towelettes nationwide after CGMP deviations were identified in manufacturing. The products carry NDC 0924-7116-03 and come in 50-wipe packages. Consumers should stop using the product and contact the company for guidance. A recall notice will be mailed to affected customers.

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
First Aid Only, 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, ACME United Corporation
Product type
BZK antiseptic towelettes
Model numbers
MN34722, MN34722B
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

First Aid Only BZK Antiseptic Towelettes are consumer healthcare items used for antiseptic cleansing. They come in 50-wipe packages and use 0.13% benzalkonium chloride. They are distributed nationwide in the United States.

Why This Is Dangerous

The hazard stems from CGMP deviations in manufacturing, not from a specific injury in the recall data. The issue relates to manufacturing quality controls rather than direct consumer harm documented in the notice.

Industry Context

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

Real-World Impact

Consumers should stop using the product and await guidance. The recall may disrupt access to a commonly used antiseptic wipe in some settings.

Practical Guidance

How to identify if yours is affected

  1. Verify NDC 0924-7116-03 on the box
  2. Check lot MN34722 or MN34722B
  3. Confirm expiration date Nov 2027 or Aug 2027

Where to find product info

Packaging, recall notice, and FDA recall page for identification codes and guidance

What timeline to expect

No replacement/refund timeline is specified in the notice. Follow ACME United Corporation’s instructions in the recall notice and FDA updates for next

If the manufacturer is unresponsive

  • Seek guidance from FDA consumer safety information
  • File a consumer complaint with FDA if the company is unresponsive

How to prevent similar issues

  • Verify NDC codes before purchase
  • Be wary of manufacturing deviations in consumer items
  • Follow recall notices from FDA and the company for updated guidance

Documentation advice

Keep the recall notice, product packaging, photos of the packaging, and any correspondence with the company

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Product Details

Product: First Aid Only BZK Antiseptic Towelettes, 50 wipes, NDC 0924-7116-03. Lot numbers include MN34722 and MN34722B. Expiration dates: Nov 2027 and Aug 2027. Distribution: Nationwide within the United States.

Key Facts

  • Lot MN34722; MN34722B
  • Exp. Date Nov 2027; Aug 2027
  • 50 wipes per package
  • Distribution nationwide in the United States
  • Recall status: ACTIVE

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
MN34722
MN34722B
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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