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Stop using now Drug recall · FDA · Published December 6, 2021

Valisa Kleantouch Hand Sanitizer Recall: Methanol Risk

Valisa recalls Kleantouch hand sanitizer with methanol due to unapproved drug status. Products labeled as 70% ethyl alcohol contain methanol and are unapproved new drugs. Consumers should check product details and contact Valisa for assistance.

🇺🇸 FDA recall #D-0363-2022DrugValisa ›
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Recalling firmValisa MFG LLC131 Executive Blvd · Farmingdale, NY 11735-4719
✎ GovInfoNow plain-language explainer

Valisa is recalling Kleantouch hand sanitizer products that contain methanol, an unapproved drug ingredient. This poses a risk of serious injury or death because methanol is toxic and not approved for human use in hand sanitizers. Read more at govinfonow.com/recall/35426-valisa-kleantouch-hand-sanitizer-recall-methanol-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/35426-valisa-kleantouch-hand-sanitizer-recall-methanol-risk · Updated August 18, 2026 · FDA enforcement record: FDA #D-0363-2022

Cite this page

“Valisa Kleantouch Hand Sanitizer Recall: Methanol Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/35426-valisa-kleantouch-hand-sanitizer-recall-methanol-risk. Based on FDA recall #D-0363-2022 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0363-2022%22&limit=1).

The FDA announced on December 6, 2021, that Valisa MFG LLC is recalling kleantouch HAND SANITIZER because the product contains methanol and is marketed without an approved New Drug Application. The agency classified the recall as Class I.

How to tell if you have it

  • Brand: Valisa
  • Product: kleantouch HAND SANITIZER (ethyl alcohol 70%), 8.0 FL OZ (236 ML), pump bottles
  • Distributed by: Valisa MFG, LLC
  • UPC: 6 86162 99246 1
  • Lot codes: 1260-1, 1260-2, 1260-3, 1260-4
  • Expiration date: 04/2022
  • Distribution: Nationwide in the USA

The hazard

The product is labeled to contain ethyl alcohol but contains methanol, making it an unapproved new drug. The FDA classified this as a Class I recall.

Context

GovInfoNow's records show other recent recalls of similar products include Zep Alcohol Sanitizer Spray Recall regarding microbial contamination risk on May 22, 2026, and OneSource Specialty Pharma Methohexital Sodium Recall concerning impurities risk serious injury on June 7, 2026. Fresenius Kabi Lidocaine HCl Injection Recall involving hair found in products occurred on July 16, 2026.

How to tell if you have this one

Check for Kleantouch hand sanitizer pump bottles labeled 'ethyl alcohol 70%', 8.0 fl oz (236 ml), with UPC 6 86162 99246 1 and lot numbers 1260-1 to 1260-4. Products were distributed by Valisa MFG LLC and made in the USA, expiring April 2022.

  • Brand
    Valisa
  • Product
    kleantouch HAND SANITIZER (ethyl alcohol 70%), 8.0 FL OZ (236 ML), pump bottles, Distributed by: Valisa MFG, LLC
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Stop Using Now

    Immediately stop using the recalled Kleantouch hand sanitizer products as they contain methanol, which is toxic and unapproved for human use.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide in the USA” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 2.2 years after the firm started it.

1. Firm started the recall: Dec 6, 202112. Published in FDA’s Enforcement Report: Jan 5, 202223. FDA classified it Class I: Jan 10, 202234. FDA terminated the recall: Feb 26, 2024420212024
  1. Firm started the recall
  2. Published in FDA’s Enforcement Report
  3. FDA classified it Class I
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #D-0363-2022 (December 6, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0363-2022 to see it in context.
  • Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA