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Green Guard Antiseptic Wipes Recall 2026 Over CGMP Deviations

Green Guard Antiseptic Wipes, distributed nationwide by ACME United Corporation, are being recalled as of January 20, 2026. FDA enforcement cites CGMP deviations in manufacturing for the benzalkonium chloride wipes, NDC 47682-056-73. Consumers and healthcare providers should stop using the product immediately and contact ACME United for guidance on refunds or replacements.

Official notice

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DRUG
Recall date
January 20, 2026
Status
ACTIVE
Severity
4/10

Quick Facts at a Glance

Recall Date
January 20, 2026
Hazard Level
HIGH
AI Risk Assessment
MEDIUM
Brands
Green Guard 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

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Green Guard Antiseptic Wipes, Unifirst First Aid Corporation
Product type
Antiseptic Wipes
Model numbers
MN15922, MN18223, MN10123, MN27223, MN01023
UPC codes
47682-056, 47682-056-99, 47682-056-73, 47682-056-33
Sizes
25 wipes per box
Sold at
Multiple Retailers
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    January 20, 2026

  2. Reported by FDA DRUG

    March 11, 2026

  3. RecallRadar source check

    March 18, 2026

  4. 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

Green Guard Antiseptic Wipes are used for cleaning minor wounds and skin disinfection in clinical and household settings.

Why This Is Dangerous

CGMP deviations indicate manufacturing process controls may not meet quality standards, potentially affecting product safety or efficacy.

Industry Context

This recall is not described as part of a broader industry pattern.

Real-World Impact

Consumers may discontinue use and seek replacements; the recall could impact distribution of antiseptic wipes across healthcare facilities and households.

Practical Guidance

How to identify if yours is affected

  1. Check packaging for the brand name Green Guard Antiseptic Wipes and NDC 47682-056-73.
  2. Look for Lot MN15922, MN18223, MN10123, MN27223, or MN01023 on the box or inner packaging.
  3. Verify Expiration Dates: Apr 2027, May 2028, Mar 2028, Aug 2028, Dec 2027.

Where to find product info

FDA recall page and ACME United Corporation recall communications.

What timeline to expect

4-8 weeks for refund or replacement processing once initiated.

If the manufacturer is unresponsive

  • File a consumer complaint with the FDA if the manufacturer is unresponsive.
  • Keep copies of all communications and the original packaging.

How to prevent similar issues

  • Verify CGMP compliance for clinical supplies before purchase.
  • Check for recall notices on manufacturer and FDA sites before using antiseptic wipes.
  • Prefer products with clear lot and expiration labeling.

Documentation advice

Keep the recall letter, packaging, receipts, and any correspondence with ACME United Corporation.

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Product Details

Brand: Green Guard Antiseptic Wipes NDC: 47682-056-73 Active ingredients: Benzalkonium chloride 0.13% Package: 25 wipes per box Distributor: ACME United Corporation Sold nationwide in the United States Lot numbers and expirations: - MN15922 (Exp Apr 2027) - MN18223 (Exp May 2028) - MN10123 (Exp Mar 2028) - MN27223 (Exp Aug 2028) - MN01023 (Exp Dec 2027)

Key Facts

  • NDC 47682-056-73 on the affected packaging
  • Lot numbers MN15922, MN18223, MN10123, MN27223, MN01023 with respective Exp dates 2027-04, 2028-05,
  • Exp 2028-03, Aug 2028, Dec 2027
  • Distributed nationwide by ACME United Corporation
  • CGMP deviations cited as reason for recall

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 LevelMEDIUM
Severity Score
4/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Details

Model Numbers
MN15922
MN18223
MN10123
MN27223
MN01023
UPC Codes
47682-056
47682-056-99
47682-056-73
+1 more
Affected States
ALL
Report Date
March 11, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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