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
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
- 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
- Antibacterial Towelette
- Model numbers
- MN24523, MN27123, MN28223
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
January 20, 2026
Reported by FDA DRUG
March 11, 2026
RecallRadar source check
March 18, 2026
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
Max Packaging Antibacterial Towelette is an antiseptic wipe used for cleaning hands and surfaces. It is sold in 4x7 packs with 1 towelette per unit.
Why This Is Dangerous
CGMP deviations refer to manufacturing process irregularities that can affect product quality. The recall warns of potential safety or efficacy concerns due to these deviations.
Industry Context
This recall is not indicated as part of a broader industry pattern.
Real-World Impact
No injuries reported to date. Nationwide distribution means consumers across the United States may have the affected product. Consumers should stop use immediately.
Practical Guidance
How to identify if yours is affected
- Check packaging for NDC 59647-750-01
- Look for Lot MN24523, MN27123, or MN28223
- Verify expiration dates: July 2028, August 2028, September 2028
- Confirm product is Max Packaging Antibacterial Towelette (Benzalkonium Chloride 0.13%)
Where to find product info
FDA recall page and ACME UNITED notices linked in the recall documentation
What timeline to expect
Not specified in recall notice
If the manufacturer is unresponsive
- Escalate with FDA recall contacts
- File a consumer complaint with CPSC if applicable
- Document all communications with the manufacturer
How to prevent similar issues
- Ask for CGMP-certified production details when buying similar products
- Check NDC numbers and expiration dates before use
- Avoid using antibacterial wipes from unknown lots or manufacturers
- Report any adverse events to FDA
Documentation advice
Keep packaging, take photos of lot and expiration dates, save recall notice and correspondence, track submission dates for refunds or replacements
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Product Details
Product: Max Packaging Antibacterial Towelette (Benzalkonium Chloride 0.13%). Form: 1 towelette. Pack size: 4x7. NDC: 59647-750-01. Lot numbers: MN24523; MN27123; MN28223. Expiration: MN24523 by July 2028; MN27123 by August 2028; MN28223 by September 2028. Manufactured in the United States. Sold nationwide in the United States. Manufacturer: ACME UNITED CORPORATION.
Key Facts
- Lot MN24523 exp July 2028
- Lot MN27123 exp August 2028
- Lot MN28223 exp September 2028
- Made in USA
- CGMP Deviations (Class II recall)
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Safety Guide
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