Quick Facts at a Glance
- Recall Date
- January 20, 2026
- Hazard Level
- HIGH
- Brands
- Medi-First Antiseptic Wipes, Unifirst First Aid 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
- Medi-First Antiseptic Wipes, Unifirst First Aid Corporation
- Product type
- Antiseptic Wipes (BZK)
- Model numbers
- MN15922, MN31022, MN27223
- UPC codes
- 47682-122, 47682-252, 47682-122-99, 47682-122-71, 47682-122-33, 47682-252-99, 47682-252-71
- Sizes
- 100 wipes per box
- 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
Medi-First Antiseptic Wipes are pre-moistened wipes used for wound cleansing and antisepsis in first aid and clinical settings.
Why This Is Dangerous
CGMP deviations raise concerns about manufacturing quality and potential impact on antiseptic efficacy.
Industry Context
This recall is not described as part of a broader industry pattern.
Real-World Impact
Users may experience reduced antiseptic effectiveness, increasing risk for inadequate wound care.
Practical Guidance
How to identify if yours is affected
- Locate the lot numbers MN15922, MN31022, MN27223 on the package.
- Verify Expiration Dates: Apr 2027, Oct 2027, Aug 2028.
- Check NDC 47682-122-33 on the label.
Where to find product info
NDC and lot numbers appear on the product packaging and carton.
What timeline to expect
Remedies such as refunds or replacements typically process in 4-6 weeks.
If the manufacturer is unresponsive
- Escalate to FDA consumer complaint portal.
- Consider state consumer protection resources.
- Document all communications and keep copies of packaging.
How to prevent similar issues
- Buy from reputable retailers with visible recall notices.
- Always verify NDC and lot codes before use or purchase.
- Retain packaging until you confirm remedy.
- Prefer products with transparent CGMP compliance statements.
Documentation advice
Keep receipts, packaging, and all recall-related correspondence.
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Product Details
Product: Medi-First Antiseptic Wipes (BZK) 0.13% benzalkonium chloride. Packaging: 100 wipes per box. Manufacturer: Medique Products, Fort Myers, FL 33967. NDC: 47682-122-33. Lots/Expirations: MN15922 (Apr 2027), MN31022 (Oct 2027), MN27223 (Aug 2028). Distribution: Nationwide in the United States. Recall date: 2026-01-20. Recall status: ACTIVE. Distributor/recall entity: ACME United Corporation.
Key Facts
- 100 wipes per box packaging
- Lot MN15922, Exp Apr 2027; MN31022, Exp Oct 2027; MN27223, Exp Aug 2028
- Manufactured for Medique Products, Fort Myers, FL 33967
- Active recall as of 2026-01-20
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Safety Guide
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