HIGHFDA DRUG

ACME UNITED Instant Hand Sanitizing Wipes Recalled for CGMP Deviations (2026)

ACME UNITED recalled instant hand sanitizing wipes nationwide after FDA flagged CGMP deviations. The product, labeled for Children’s Healthcare of Atlanta and manufactured in the USA, contains benzalkonium chloride 0.13% and is sold 1,000 wipes per case under NDC 0924-7130-00. Consumers and healthcare providers should stop using this product immediately and contact ACME UNITED CORPORATION for next

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
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
Instant Hand Sanitizing Wipes
Model numbers
MN12122, MN27523, MN30922
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

These wipes are marketed as instant hand sanitizing products used for quick sanitization in healthcare settings. The package label references 1000 wipes per case and a benzalkonium chloride active ingredient.

Why This Is Dangerous

CGMP deviations indicate manufacturing quality issues that could affect product safety or efficacy, though no specific adverse events are reported in the notice.

Industry Context

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

Real-World Impact

Facilities and consumers should discontinue use to avoid potential quality-related risks. The recall may affect purchasing decisions for healthcare cleaning supplies and hand hygiene products.

Practical Guidance

How to identify if yours is affected

  1. Inspect packaging for NDC 0924-7130-00 and the lot numbers MN12122, MN27523, MN30922.
  2. Verify expiration dates Apr 2027, Aug 2028, Oct 2027.
  3. Cross-check against the FDA recall page for updates.

Where to find product info

NDC on the package label and lot numbers on the wrap. FDA recall page linked in notice.

What timeline to expect

No refund/replacement timeframe published. Watch for official guidance and corporate communications.

If the manufacturer is unresponsive

  • File a complaint with the FDA recall program if ACME UNITED does not respond within a reasonable timeframe.
  • Consider contacting consumer protection agencies for guidance.

How to prevent similar issues

  • Vet suppliers for CGMP compliance before purchase.
  • Prefer products with transparent manufacturing records and recent recalls avoided.
  • Look for up-to-date FDA recall notices for any medical or personal care items.

Documentation advice

Save the recall notice and any correspondence with the manufacturer. Photograph lot codes, expiration dates, and packaging for records.

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Product Details

Product: ACME UNITED Instant Hand Sanitizing Wipes NDC: 0924-7130-00 Labeling: Children’s Healthcare of Atlanta Case quantity: 1000 wipes per case Model/Lot numbers: MN12122, MN27523, MN30922 Expiration dates: Apr 2027, Aug 2028, Oct 2027 Manufactured for: Food Service Resources, Flowery Branch, GA 30542, USA Distribution: Nationwide within the United States Recall date: 2026-01-20 Status: ACTIVE Notes: Sold nationwide; no pricing information available

Key Facts

  • 1000 wipes per case
  • Lot MN12122; Exp Apr 2027
  • Lot MN27523; Exp Aug 2028
  • Lot MN30922; Exp Oct 2027
  • 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
4/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
MN12122
MN27523
MN30922
Affected States
ALL
Report Date
March 11, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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