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Lower risk Drug recall · FDA · Published September 21, 2021

Sanitor Cleaning Solutions Foaming Hand Sanitizer Recall: Skin Irritation Risk

Sanitor Corporation recalls foaming hand sanitizer with benzalkonium chloride 0.1% due to possible skin irritation and infection risks. Affected lots expire Sept 2021.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #D-0018-2022DrugSanitor Corporation ›
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Contact the company

Recalling firmSanitor Corporation8400 Cerritos Ave · Stanton, CA 90680-2504
✎ GovInfoNow plain-language explainer

Sanitor Corporation is recalling foaming hand sanitizers that may cause skin irritation or infection. This recall affects products with specific lot numbers and expiration dates. Read more at govinfonow.com/recall/35849-sanitor-cleaning-solutions-foaming-hand-sanitizer-recall-skin-irritation-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/35849-sanitor-cleaning-solutions-foaming-hand-sanitizer-recall-skin-irritation-risk · Updated August 18, 2026 · FDA enforcement record: FDA #D-0018-2022

Cite this page

“Sanitor Cleaning Solutions Foaming Hand Sanitizer Recall: Skin Irritation Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/35849-sanitor-cleaning-solutions-foaming-hand-sanitizer-recall-skin-irritation-risk. Based on FDA recall #D-0018-2022 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0018-2022%22&limit=1).

The FDA announced on Sept. 21, 2021, that Sanitor Corporation voluntarily recalled Cleaning Solutions Foaming Hand Sanitizer due to current good manufacturing practice deviations. The agency stated the product may cause skin or soft tissue infection and irritation.

How to tell if you have it

  • Brand: Sanitor Corporation
  • Product: Cleaning Solutions Foaming Hand Sanitizer, Active Ingredient Benzalkonium chloride 0.1%, New Wave Cleaning Solutions
  • UPC: 8 60001 93396 3
  • Lot codes: 20102, 20103
  • Expiration: September 2021
  • Distribution: One distributor in Las Vegas, NV

The hazard

According to the FDA, current good manufacturing practice deviations in this product may cause possible infection or irritation of the skin and/or soft tissues.

Context

GovInfoNow's records show other recent recalls include ACME Children's Hand Sanitizer Wipes (Jan. 20, 2026) and Owen Biosciences Night Lotion (March 3, 2026). Keystone Dental City Topical Anesthetic Gel was also recalled on May 21, 2026.

How to tell if you have this one

Check for lot numbers 20102 or 20103 on the product label. The product expires in September 2021 and is sold by Sanitor Corporation in Las Vegas, Nevada.

  • Brand
    Sanitor Corporation
  • Product
    Cleaning Solutions Foaming Hand Sanitizer, Active Ingredient Benzalkonium chloride 0.1%, New Wave Cleaning Solutions
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for lot numbers 20102 or 20103 on the product label.

Where it went and when

Where it was distributed

Distributed in Nevada.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: yesNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “Distributed to one distributor located in Las Vegas, NV.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Nevada.

Recall timeline

FDA terminated this recall 19 months after the firm started it.

1. Firm started the recall: Sep 21, 202112. FDA classified it Class II: Oct 15, 202123. Published in FDA’s Enforcement Report: Oct 27, 202134. FDA terminated the recall: Apr 21, 2023420212023
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  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-0018-2022 (September 21, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0018-2022 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