HIGH

ACME United WP WipesPlus Hand Sanitizing Wipes 100 CT Recalled for CGMP Deviations (2026)

ACME United recalled WP WipesPlus Hand Sanitizing Wipes, 100-count, sold nationwide, after CGMP deviations were identified. The recall is classified as Class II. Consumers should stop using the product immediately and await guidance from ACME United. The NDC is 67151-727-01.

Quick Facts at a Glance

Recall Date
January 20, 2026
Hazard Level
HIGH
Brands
ACME United, Progressive Products
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

WP WipesPlus Hand Sanitizing Wipes are designed for on-the-go hand sanitation. The wipes are 5x7 inches with benzalkonium chloride as the active ingredient and sold in 100-count packages.

Why This Is Dangerous

The recall is due to CGMP deviations in manufacturing. It is a quality-control issue rather than an identified chemical hazard in consumer exposure reports to date.

Industry Context

This recall is not described as part of a broader industry pattern in the provided notice.

Real-World Impact

Consumers may face delays or inconvenience in replacing a recalled product. There is no reported injury at this time, but the recall could affect product safety or effectiveness if CGMP deviations impact purity or packaging.

Practical Guidance

How to identify if yours is affected

  1. Check the package for WP WipesPlus Hand Sanitizing Wipes, 100 CT
  2. Verify the active ingredient is Benzalkonium Chloride 0.13%
  3. Confirm size 5x7 inches and NDC 67151-727-01
  4. Look for Lot numbers MN27922, MN21722, MN21822, MN27422, MN27522, MN25422
  5. Check expiration dates Jul 2027, Sep 2027, Aug 2027

Where to find product info

Lot numbers and expiration dates printed on the packaging. Official recall details at FDA enforcement page D-0372-2026.

What timeline to expect

Refunds or replacements typically processed within 4-6 weeks after eligibility verification.

If the manufacturer is unresponsive

  • Document all communications with ACME United
  • File a complaint with the CPSC if there is no resolution after a reasonable period
  • Consult healthcare professionals if exposure or use concerns arise

How to prevent similar issues

  • Check packaging for the NDC and lot codes when buying sanitizing wipes
  • Prefer products with clear CGMP compliance documentation
  • Buy from reputable retailers with recall information available
  • Keep receipts and packaging until resolution is complete

Documentation advice

Keep the product, packaging, recall notice, and all correspondence with the manufacturer or retailer for records.

Product Details

Product: WP WipesPlus Hand Sanitizing Wipes. Active ingredient: Benzalkonium Chloride 0.13%. Size: 5x7 inches. Count: 100 per package. Brand/Manufacturer: Progressive Products. Distributor: ACME United Corporation. Address on filing: 211 S. Ridge Street, Rye Brook, NY 10573. Sold nationwide in the United States. NDC: 67151-727-01. Recall date: 2026-01-20. Status: ACTIVE. Model/Lot numbers include MN27922, MN21722, MN21822, MN27422, MN27522, MN25422. Expiration dates listed: Jul 2027, Sep 2027, Aug 2027. Remedial action: Stop use and contact ACME United for guidance. Reminder: Notification by (

Key Facts

  • 100-count packages
  • 5x7 inch wipes
  • Benzalkonium Chloride 0.13%
  • NDC 67151-727-01
  • Lot numbers MN27922, MN21722, MN21822, MN27422, MN27522, MN25422
  • Exp. dates Jul 2027, Sep 2027, Aug 2027

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
5/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Details

Model Numbers
MN27922
MN21722
MN21822
MN27422
MN27522
+4 more
Affected States
ALL
Report Date
March 11, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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