HIGHFDA DRUG

ACME United BZK Antiseptic Towelettes Recall for CGMP Deviations (2026)

ACME United Corporation recalled BZK Antiseptic Towelettes sold for Food Service Resources nationwide after CGMP deviations were found. The recall is Class II and high risk. Consumers and healthcare providers should stop using this product immediately and follow recall 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
Brand
ACME United
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
ACME United
Product type
BZK Antiseptic Towelettes
Model numbers
MN22222, MN05523, MN32023, MN15523, MN11422, MN11422B, MN03823, MN09223 +4 more
Sizes
5x7 inches
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

BZK antiseptic towelettes are single-use wipes used to sanitize hands in healthcare and food-service environments. They come in bulk packaging for institutional use and are labeled with NDC 0924-7130-00.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

The recall may affect hand sanitation practices in healthcare and food-service settings. No injuries are reported in this notice. Consumers should stop using the product until guidance is received.

Practical Guidance

How to identify if yours is affected

  1. Check if your package lists NDC 0924-7130-00
  2. Confirm 5x7 inch size and 1,000 count bulk packaging

Where to find product info

Identifiers appear on outer packaging and inner packaging. NDC and lot numbers appear near product description and lot code area.

What timeline to expect

Refund or replacement processing typically 4-6 weeks after submission.

If the manufacturer is unresponsive

  • Document your recall notice and any communications
  • Escalate to FDA recall contact if the company is unresponsive
  • File a consumer complaint with CPSC if applicable

How to prevent similar issues

  • Check NDC numbers before purchase in the future
  • Prefer products with transparent CGMP certification signals or audited facilities
  • Keep product batch information for recalls

Documentation advice

Keep copies of the recall letter, photos of packaging showing NDC and lot codes, and correspondence with the manufacturer.

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Product Details

Product: BZK Antiseptic Towelettes, benzalkonium chloride 0.13%, 5x7 inches. Packaging: bulk 1,000 ea. Made in USA for Food Service Resources, Flowery Branch, GA 30542. NDC 0924-7130-00. Variants listed include Piedmont Sanitizing Hand Wipes, Touchpoint, Wellstar Cobb Hand Wipes, FSR Sanitizing Hand Wipes, and Children’s 5x7 inch wipes. Inner packaging: Instant Hand Sanitizing Wipes. Distribution: Nationwide in the United States.

Key Facts

  • 5x7 inch towels
  • Exp dates include Jul 2027, Jan 2028, Oct 2028, May 2028, Mar 2027, Mar 2028, Apr 2028, Jun 2028, 0
  • Nationwide US distribution

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 Details

Model Numbers
MN22222
MN05523
MN32023
MN15523
MN11422
+7 more
Affected States
ALL
Report Date
March 11, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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