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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Drug
Medications & Supplements/Topical Products

Klean Touch Hand Sanitizer Recalled for Methanol Contamination

Agency Publication Date: December 28, 2021
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Summary

Aroma Release Technologies Inc is recalling 37 55-gallon drums of Klean Touch Hand Sanitizer (Ethyl Alcohol 70%) because the product was found to be contaminated with methanol. The product's label even listed methanol as an ingredient, which is not permitted in hand sanitizers and makes the product an unapproved new drug. No incidents or injuries have been reported to date, but the contaminated sanitizer was distributed to customers in Texas and New York.

Risk

Methanol, or wood alcohol, is a toxic substance that is not safe for use in hand sanitizers. Exposure to methanol through the skin or by accidental ingestion can lead to serious health issues including nausea, blurred vision, blindness, seizures, coma, permanent damage to the nervous system, or death.

What You Should Do

  1. The recalled product is Klean Touch Hand Sanitizer (Ethyl Alcohol 70%) sold in 55-gallon drums by Aroma Release Technology, Inc. This recall involves lot numbers 1620-1, 1620-3, 1620-4, 1820-4, 1820-5, 1920-1, and 1920-2, all of which are labeled as having no expiration date.
  2. Check the labels on any industrial-sized 55-gallon hand sanitizer drums to see if they identify as the 'Klean Touch' brand and match one of the seven lot numbers listed above.
  3. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact Aroma Release Technologies Inc for further instructions.
  4. For additional questions, call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA).

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Klean Touch Hand Sanitizer (Ethyl Alcohol 70%) (55-gallon drum)by Klean Touch
Variants: 55-gallon drum
Lot Numbers:
1620-1 (No Expiration Date)
1620-3 (No Expiration Date)
1620-4 (No Expiration Date)
1820-4 (No Expiration Date)
1820-5 (No Expiration Date)
1920-1 (No Expiration Date)
1920-2 (No Expiration Date)

Ingredients labeled as containing Ethanol and Methanol; manufactured by Aroma Release Technology, Inc. in Chattanooga, TN.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 89138
Status: Resolved
Manufacturer: Aroma Release Technologies Inc
Sold By: Aroma Release Technology, Inc.
Manufactured In: United States
Units Affected: 37 55-gallon drums
Distributed To: Texas, New York

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.