HIGH

ACME United Recalls Wipes Plus Hand Sanitizing Alcohol Free BZK Wipes (2026)

ACME United recalled Wipes Plus Hand Sanitizing Alcohol Free BZK Wipes sold nationwide on Jan. 20, 2026. The recall cites CGMP deviations in manufacturing. Consumers and healthcare providers should stop using the product immediately and contact ACME United or their healthcare provider for guidance.

Quick Facts at a Glance

Recall Date
January 20, 2026
Hazard Level
HIGH
Brand
ACME United
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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Product Details

Product: Wipes Plus Hand Sanitizing Alcohol Free BZK Wipes (0.13% benzalkonium chloride). NDC: 67151-333-01. Manufactured for: CFS Brands DBA WipesPlus, 4711 E. Heiner Rd., Oklahoma City, OK 73331. Distribution: Nationwide in the United States. Sold at: Nationwide across multiple retailers. Recall date: 2026-01-20. Status: Active. Class: II. Model numbers: MN16022, MN33922, MN31222, MN16522, MN17022, MN03323, MN34622. Expiration dates in the lot listings: Aug 2027, Apr 2027, Oct 2027, Jan 2028. Note: Quantity not disclosed.

The Hazard

Hazard type listed as CGMP Deviations. Deviation in current good manufacturing practices could affect product quality and safety. The recall does not specify a chemical or physical defect beyond GMP concerns.

What to Do

1. Stop using the product immediately. 2. Contact ACME United Corporation or your healthcare provider for guidance. 3. Expect a recall notification by letter with further instructions.

Contact Information

Removal or guidance contact is listed through the FDA recall page. For official details, see the recall notice at the FDA enforcement site. Hours and direct phone contact for ACME United are not provided in the available data.

Key Facts

  • NDC 67151-333-01
  • Model numbers MN16022, MN33922, MN31222, MN16522, MN17022, MN03323, MN34622
  • Expirations: Aug 2027, Apr 2027, Oct 2027, Jan 2028
  • Recall date 2026-01-20
  • Status ACTIVE
  • Distribution Nationwide

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
MN16022
MN33922
MN31222
MN16522
MN17022
+2 more
Affected States
ALL
Report Date
March 11, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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