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
- Hand Sanitizing Wipe
- Model numbers
- MN16022, MN33922, MN31222, MN16522, MN17022, MN03323, MN34622
- 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
Why This Is Dangerous
CGMP deviations imply manufacturing practices did not meet FDA standards, potentially impacting product quality. The recall does not list a specific chemical or physical hazard in the documentation.
Industry Context
This recall is not described as part of a broader industry-wide pattern in the provided data.
Real-World Impact
Consumers may need to replace or return affected wipes. The recall is active nationwide, and affected individuals should follow recall guidance to avoid potential substandard products.
Practical Guidance
How to identify if yours is affected
- Check NDC 67151-333-01 on product packaging or carton
- Match model numbers MN16022, MN33922, MN31222, MN16522, MN17022, MN03323, MN34622 and expiration dates Aug 2027, Apr 2027, Oct 2027, Jan 2028
- Note lot identifiers like MN16022 on the packaging
What timeline to expect
4-8 weeks for refunds/replacements after submission
If the manufacturer is unresponsive
- Escalate to FDA via recall page
- File a consumer complaint with your state attorney general
- Consult a legal professional if you experience injuries
How to prevent similar issues
- Only purchase from reputable retailers
- Look for CGMP-compliant manufacturing indicators on product pages
- Verify NDC and model numbers before use
- Register product recalls with your household inventory
Documentation advice
Keep product packaging, take photos of lot numbers and expiration dates, maintain recall notices and correspondence
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Product Details
Product: Wipes Plus Hand Sanitizing Alcohol Free BZK Wipes (0.13% benzalkonium chloride). NDC: 67151-333-01. Manufactured for: CFS Brands DBA WipesPlus, 4711 E. Heiner Rd., Oklahoma City, OK 73331. Distribution: Nationwide in the United States. Sold at: Nationwide across multiple retailers. Recall date: 2026-01-20. Status: Active. Class: II. Model numbers: MN16022, MN33922, MN31222, MN16522, MN17022, MN03323, MN34622. Expiration dates in the lot listings: Aug 2027, Apr 2027, Oct 2027, Jan 2028. Note: Quantity not disclosed.
Key Facts
- Expirations: Aug 2027, Apr 2027, Oct 2027, Jan 2028
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Safety Guide
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