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ACME United Savannah Antibacterial Towelettes Recalled for CGMP Deviations (2026)

ACME United Corporation is recalling Savannah Antibacterial Towelettes nationwide after CGMP deviations in manufacturing. The deviations may affect product quality and safety. Stop using the product immediately and contact ACME United or your healthcare provider for guidance.

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
7/10

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

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
ACME UNITED
Product type
Antibacterial Towelettes
Model numbers
MN24623, MN27023, MN32423, MN300724
Sizes
1 towelette, 4 x 7 inches
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

Savannah Towelettes are single-towelette cleaning and disinfecting products sold in a dispensing format. They are used for hand or surface cleaning with benzalkonium chloride as the active ingredient.

Why This Is Dangerous

CGMP deviations indicate manufacturing quality controls did not meet current standards. This may affect product consistency, potency, or contamination risk, though no specific injuries are reported.

Industry Context

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

Practical Guidance

How to identify if yours is affected

  1. Check NDC 59647-749-02 on the product package.
  2. Verify lot numbers MN24623, MN27023, MN32423, or MN300724.
  3. Confirm expiration dates: Jul 2028, Aug 2028, Oct 2028, or Dec 2028.

Where to find product info

FDA recall page and ACME United notices; use the provided enforcement report link for details.

What timeline to expect

Refunds or replacements are not expressly time-limited in the notice; typical recalls take several weeks to process.

If the manufacturer is unresponsive

  • Follow up with the FDA recall page for updates.
  • Consider filing a consumer complaint with the CPSC if the company is unresponsive.

How to prevent similar issues

  • When buying antibacterial products, verify CGMP compliance and keep batch information.
  • Store products in a cool, dry place and inspect expiration dates before purchase.

Documentation advice

Save the recall notice, take photos of the packaging showing NDC and lot numbers, keep receipts if available, and maintain any correspondence with the manufacturer.

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Product Details

Product: Savannah Antibacterial Towelettes (Benzalkonium Chloride 0.13%), 1 towelette, 4 x 7. NDC: 59647-749-02. Brand: Savannah. Lot numbers: MN24623 (Exp Jul 2028), MN27023 (Exp Aug 2028), MN32423 (Exp Oct 2028), MN300724 (Exp Dec 2028). Distributed nationwide in the United States. Recall date: 2026-01-20. Status: Active. Manufacturer: ACME United Corporation. Packaging: 1 towelette per packet, 4 x 7 inches. Sold through multiple retailers.

Key Facts

  • Active recall status as of 2026-03-11
  • NDC 59647-749-02 associated with four lots
  • Expirations: Jul 2028, Aug 2028, Oct 2028, Dec 2028
  • Hazard: CGMP Deviations in manufacturing

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
MN24623
MN27023
MN32423
MN300724
Affected States
ALL
Report Date
March 11, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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