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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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High RiskFDA Drug
Medications & Supplements/Topical Products

Nanomateriales Sa De Cv: Zanilast+ Antiseptic Hand Sanitizer Recalled for Potential 1-Propanol

Agency Publication Date: October 6, 2020
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Summary

Approximately 20,440 units of Zanilast+ Gel Antiseptic Hand Sanitizer (70% Ethyl Alcohol) are being recalled due to manufacturing deviations that could lead to the presence of 1-propanol. This recall affects various sizes including 1-liter bottles, 1-gallon bottles, and 25 kg containers sold in California, New York, and Mexico. Consumers should check their supply for all lots of this product, as it was found to potentially contain toxic levels of 1-propanol rather than the safe ethyl alcohol listed on the label.

Risk

1-propanol is a toxic substance that can cause central nervous system depression, leading to symptoms like confusion, decreased consciousness, and slowed breathing. While it is intended for skin use, accidental ingestion or absorption through the skin of 1-propanol can be life-threatening, particularly for children.

What You Should Do

  1. Immediately check your supply for Zanilast+ Gel Antiseptic Hand Sanitizer in 1-liter (33.8 fl oz), 1-gallon (3.76L), or 25 kg bottles.
  2. Identify affected 1-liter bottles by looking for NDC 69912-008-01 and UPC 2 000000 531151.
  3. Identify affected 1-gallon bottles by looking for NDC 69912-008-02 and UPC 2 000000 531144.
  4. Identify affected 25 kg containers by looking for NDC 69912-006-01.
  5. Stop using these products immediately and contact a healthcare provider or pharmacist if you have experienced any adverse health effects.
  6. Return any unused product to the place of purchase for a full refund and contact the manufacturer, Nanomateriales Sa De Cv, for further instructions.
  7. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA).

Your Remedy Options

๐Ÿ’ฐFull Refund

Contact healthcare provider and return product for refund.

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: Zanilast+ Gel Antiseptic Hand Sanitizer (1L / 33.8 fl oz)
Model:
NDC 69912-008-01
UPC Codes:
2000000531151
Lot Numbers:
All lots
Product: Zanilast+ Gel Antiseptic Hand Sanitizer (1 gal / 3.76L)
Model:
NDC 69912-008-02
UPC Codes:
2000000531144
Lot Numbers:
All lots
Product: Zanilast+ Gel Antiseptic Hand Sanitizer (25 kg)
Model:
NDC 69912-006-01
Lot Numbers:
All lots

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 86333
Status: Resolved
Manufacturer: Nanomateriales Sa De Cv
Sold By: Fujimura Trading S.A. DE C.V.
Manufactured In: Mexico
Units Affected: 2 products (a)19,440 liters b) 25,917 gallon; 1,000 kg)
Distributed To: California, 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.