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Unrated Drug recall · FDA · Published August 18, 2020

Nanomateriales Zanilast+ Hand Sanitizer Recall: Potential 1-Propanol Contamination

Nanomateriales recalls Zanilast+ Gel Antiseptic Hand Sanitizer (70% Ethyl Alcohol) due to potential 1-propanol contamination. All lots are affected. Consumers should check product labels for NDC 69912-008-01 or 69912-008-02.

🇺🇸 FDA recall #D-1592-2020DrugNanomateriales ›
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Contact the company

Recalling firmNanomateriales Sa De CvAvenida Milimex 215, Col. Milimex, Apodaca · Ciudad Apodaca, Mexico
✎ GovInfoNow plain-language explainer

What happened, in plain English

Nanomateriales is recalling Zanilast+ Gel Antiseptic Hand Sanitizer products that may contain 1-propanol. This chemical could pose a risk to health, especially for sensitive individuals or those with certain medical conditions. Read more at govinfonow.com/recall/36831-nanomateriales-zanilast-hand-sanitizer-recall-potential-1-propanol-contamination.

Source Summary by GovInfoNow · govinfonow.com/recall/36831-nanomateriales-zanilast-hand-sanitizer-recall-potential-1-propanol-contamination · Updated October 5, 2026 · FDA enforcement record: FDA #D-1592-2020

Cite this page

“Nanomateriales Zanilast+ Hand Sanitizer Recall: Potential 1-Propanol Contamination.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/36831-nanomateriales-zanilast-hand-sanitizer-recall-potential-1-propanol-contamination. Based on FDA recall #D-1592-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1592-2020%22&limit=1).

Why it’s dangerous

The product may contain 1-propanol, a chemical that can cause irritation or adverse reactions in some individuals. This risk is particularly concerning for people with sensitive skin or certain medical conditions.

Who’s affected

All owners of Zanilast+ Gel Antiseptic Hand Sanitizer products with NDC numbers 69912-008-01 or 69912-008-02 are affected. People with alcohol sensitivity or specific health conditions may be at higher risk.

How to tell if you have this one

Check for product labels with NDC 69912-008-01 (33.8 fl oz) or NDC 69912-008-02 (1 gal) on the bottle. The product is distributed by Fujimura Trading S.A. DE C.V. in Mexico.

  • Brand
    Nanomateriales
  • Product
    Zanilast+ Gel Antiseptic Hand Sanitizer (70% Ethyl Alcohol) Packaged in a) 33.8 fl oz (1.06 qt) (1L) (NDC 69912-008-01
  • Category
    Drug
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Terminated
  • Distribution
    CA, NY and Mexico
Recall numberProduct, codes & lotsQuantity
D-1592-2020Zanilast+ Gel Antiseptic Hand Sanitizer (70% Ethyl Alcohol) Packaged in a) 33.8 fl oz (1.06 qt) (1L) (NDC 69912-008-01 UPC 2 000000 531151); b) 1 gal (3.76L) (NDC 69912-008-02 UPC 2 000000 531144) bottles, Distributed by Fujimura Trading S.A. DE C.V. Juventino Rosas 1902, Col. Caracol, 64810, Monterrey, N.L., Mexico Nanomateriales S.A. DE C.V.; All lotsa)19,440 liters b) 25,917 gallon
D-1593-2020Zanilast+ Gel Antiseptic Hand Sanitizer (70% Ethyl Alcohol) Packaged in 25 kg bottles, Distributed by Fujimura Trading S.A. DE C.V. Juventino Rosas 1902, Col. Caracol, 64810, Monterrey, N.L., Mexico Nanomateriales S.A. DE C.V. NDC 69912-006-01; All lots1,000 kg
Based on the official FDA remedy

What to do — step by step

  1. Check Product Labels

    Look for NDC numbers 69912-008-01 or 69912-008-02 on the bottle to confirm if the product is recalled.

Where it went and when

Where it was distributed

Distributed in California and New York, and outside the U.S.

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: yesNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: 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: “CA, NY and Mexico” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California, New York.

Recall timeline

FDA terminated this recall 3.9 years after the firm started it.

1. Firm started the recall: Aug 18, 202012. FDA classified it Class II: Sep 23, 202023. Published in FDA’s Enforcement Report: Sep 30, 202034. FDA terminated the recall: Jul 5, 2024420202024
  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-1592-2020 (August 18, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1592-2020 to see it in context.
  • Plain-language summary written by qwen3:4b on October 5, 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