HIGHFDA DRUG

First Aid Only BZK Antiseptic Towelettes Recall for CGMP Deviations (2026)

First Aid Only BZK Antiseptic Towelettes are recalled nationwide in 2026 after CGMP Deviations were identified at the Acme United Corporation facility. The recall cites CGMP Deviations that could affect product quality. Consumers should stop using the product 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
8/10

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
Antiseptic Towelettes (BZK 0.13%)
Model numbers
MN12121, MN13521, MN15221, MN16721, MN16921, MN17021, MN17021B, MN18521 +7 more
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

    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

First Aid Only BZK Antiseptic Towelettes are disposable wipes containing benzalkonium chloride used for first aid. The product is distributed nationwide in the United States and is marketed under the First Aid Only brand.

Why This Is Dangerous

The recall centers on CGMP Deviations in manufacturing. This is a quality-control issue that could affect product consistency or purity, not an identified specific injury 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 immediately to avoid potential quality concerns. The recall's impact is logistical and precautionary rather than tied to reported injuries.

Practical Guidance

How to identify if yours is affected

  1. Verify NDC 0924-7116-00 on the package.
  2. Confirm product size is 5x7 bulk pack and note the label indicates First Aid Only BZK Antiseptic Towelettes.

Where to find product info

FDA recall page: https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=D-0361-2026

What timeline to expect

No timeline is stated for refunds or replacements; monitor the FDA page for updates.

If the manufacturer is unresponsive

  • Document all communication attempts with Acme United Corporation.
  • If the company is slow to respond, contact the FDA or CPSC for guidance and file a complaint if necessary.

How to prevent similar issues

  • Verify GMP compliance when buying antiseptic products.
  • Keep packaging and lot numbers for recalls.
  • Buy from reputable retailers and check for recall notices before use.

Documentation advice

Save the recall notice, take photos of packaging with lot and NDC numbers, keep receipts if available, and log all correspondence with the manufacturer.

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Product Details

Model numbers: MN12121, MN13521, MN15221, MN16721, MN16921, MN17021, MN17021B, MN18521, MN18621, MN18621B, MN24721, MN25021, MN01123, MN27421, MN27721. Lot numbers: MN12121, MN13521, MN15221, MN16721, MN16921, MN17021, MN17021B, MN18521, MN18621, MN18621B, MN24721, MN25021, MN01123, MN27421, MN27721. Expiration dates include Apr 2026, May 2026, Jun 2026, Dec 2027. Sold nationwide in the United States. Price not specified. NDC 0924-7116-00. Made in USA.

Key Facts

  • CGMP Deviations noted
  • Active recall status as of 2026-03-11
  • Nationwide US distribution
  • Bulk 5x7 towelettes
  • Made in USA

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
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Details

Model Numbers
MN12121
MN13521
MN15221
MN16721
MN16921
+10 more
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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