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
- 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
- First Aid Only BZK Antiseptic, Acme United Corporation
- Product type
- BZK Antiseptic Towelettes (0.13%)
- Model numbers
- MN26222, MN34722, MN25922, MN00523
- 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.
Recall announced
January 20, 2026
Reported by FDA DRUG
March 11, 2026
RecallRadar source check
April 13, 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
The product is a benzalkonium chloride–based antiseptic towlette used for wound cleansing and cleaning skin. It comes in boxes of 100 wipes and is sold under the First Aid Only BZK Antiseptic brand.
Why This Is Dangerous
CGMP deviations indicate potential quality-control issues in manufacturing. The recall focuses on manufacturing process concerns rather than an explicit chemical hazard from use.
Industry Context
This recall is not described as part of a broader industry pattern.
Real-World Impact
Consumers may need to discard affected lots and seek guidance from the company. There is potential inconvenience and cost associated with replacing the product.
Practical Guidance
How to identify if yours is affected
- Identify NDC 0924-7116-04 on the packaging.
- Check lot numbers MN26222, MN34722, MN25922, MN00523.
- Confirm expiration dates November 2027 or December 2027.
Where to find product info
Packaging should display NDC, lot numbers, and expiration date; the FDA recall page provides official details.
What timeline to expect
Refund or replacement timelines typical for recalls are 4-8 weeks, though official timelines may vary by company.
If the manufacturer is unresponsive
- Document all communications with ACME United and retailers.
- File a complaint with the CPSC if you encounter delays or lack of resolution.
- Consider consulting a consumer attorney for serious issues.
How to prevent similar issues
- When shopping for antiseptic products, verify CGMP compliance and check for recall notices.
- Inspect packaging for NDC codes and lot numbers before purchase.
- Buy from reputable retailers and keep receipts for possible recalls.
Documentation advice
Keep product packaging, lot numbers, expiration dates, purchase receipts, and all recall correspondence as part of your records.
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Product Details
Model numbers and identifiers include MN26222, MN34722, MN25922, MN00523. NDC 0924-7116-04. Sold nationwide in the United States. Quantity recalled: 212,607,900 containers. Recall date: 2026-01-20. Manufacturer: Acme United Corporation.
Key Facts
- Expiration dates Nov 2027 and Dec 2027
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Safety Guide
Not sure what to do next? Our guide walks you through the process step by step.
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