HIGH

Medi-First Antiseptic Wipes Recalled for CGMP Deviations in 2026, 100 Wipes per Box

ACME United Corporation recalled Medi-First Antiseptic Wipes sold nationwide in the United States. The recall cites CGMP deviations that could affect product quality. Consumers and healthcare providers should stop using the wipes immediately and contact ACME United Corporation or a healthcare provider for guidance.

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

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

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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

  1. Locate the lot numbers MN15922, MN31022, MN27223 on the package.
  2. Verify Expiration Dates: Apr 2027, Oct 2027, Aug 2028.
  3. 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.

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
  • NDC 47682-122-33
  • 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

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
7/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Details

Model Numbers
MN15922
MN31022
MN27223
UPC Codes
47682-122
47682-252
47682-122-99
+4 more
Affected States
ALL
Report Date
March 11, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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