HIGH

ACME UNITED Instant Hand Sanitizing Wipes Recalled for CGMP Deviations (2026)

ACME UNITED recalled instant hand sanitizing wipes nationwide after FDA flagged CGMP deviations. The product, labeled for Children’s Healthcare of Atlanta and manufactured in the USA, contains benzalkonium chloride 0.13% and is sold 1,000 wipes per case under NDC 0924-7130-00. Consumers and healthcare providers should stop using this product immediately and contact ACME UNITED CORPORATION for next

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: ACME UNITED Instant Hand Sanitizing Wipes NDC: 0924-7130-00 Labeling: Children’s Healthcare of Atlanta Case quantity: 1000 wipes per case Model/Lot numbers: MN12122, MN27523, MN30922 Expiration dates: Apr 2027, Aug 2028, Oct 2027 Manufactured for: Food Service Resources, Flowery Branch, GA 30542, USA Distribution: Nationwide within the United States Recall date: 2026-01-20 Status: ACTIVE Notes: Sold nationwide; no pricing information available

The Hazard

The recall centers on CGMP deviations in manufacturing. The defect relates to quality control practices rather than an explicit product hazard such as a chemical exposure or contamination described in the notice. Consumers should treat this as a quality issue that could affect product safety if manufacturing controls are not consistent.

What to Do

1. Stop using the product immediately. 2. Check lot numbers MN12122, MN27523, MN30922 and expiration dates Apr 2027, Aug 2028, Oct 2027 to determine if affected. 3. Contact ACME UNITED CORPORATION for guidance or your healthcare provider for instructions. 4. Monitor for recall updates from the FDA and from ACME UNITED. 5. If you need a remedy, follow the recall letter and official guidance. Refund or replacement details are not specified in the notice.

Contact Information

FDA recall page: https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=D-0377-2026 Manufacturer: ACME UNITED CORPORATION (recall communications via the FDA notice) Hours: Not specified in the recall notice

Key Facts

  • 1000 wipes per case
  • NDC 0924-7130-00
  • Lot MN12122; Exp Apr 2027
  • Lot MN27523; Exp Aug 2028
  • Lot MN30922; Exp Oct 2027
  • Distributed nationwide in the United States

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
4/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
MN12122
MN27523
MN30922
Affected States
ALL
Report Date
March 11, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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