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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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Medium RiskFDA Drug
Medications & Supplements/Topical Products

POLARIZED LLC: Saniderm Advanced Hand Sanitizer Recalled for Methanol Contamination

Agency Publication Date: July 28, 2020
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Summary

POLARIZED LLC is recalling approximately 18,126 bottles of Saniderm ADVANCED HAND SANITIZER (70% Alcohol Content) sold in 1-liter bottles. The recall was initiated because the product was found to contain undeclared methanol and has lower ethanol levels than the label claims. Consumers who have this product should immediately stop using it and contact a healthcare professional if they have experienced any symptoms related to methanol poisoning.

Risk

Methanol, or wood alcohol, is a toxic substance that can be absorbed through the skin or ingested; substantial exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system, or death.

What You Should Do

  1. Check your hand sanitizer bottles to see if they are 'Saniderm ADVANCED HAND SANITIZER, 70% Alcohol Content' in 1-liter bottles.
  2. Identify the affected product by looking for UPC 8 60003 63391 5 and Lot number 53131626 or any other lot produced by Eskbiochem SA de CV.
  3. Immediately stop using the hand sanitizer if it matches the recalled product details.
  4. Contact your healthcare provider or pharmacist for guidance regarding potential exposure or health concerns.
  5. Return any unused product to the place of purchase for a refund and contact POLARIZED LLC for further instructions.
  6. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

💰Full Refund

Healthcare consultation and refund

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

Affected Products

Product: Saniderm ADVANCED HAND SANITIZER (1 Liter)
Model:
D-1412-2020
UPC Codes:
860003633915
Lot Numbers:
53131626
all lots

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 85944
Status: Resolved
Manufacturer: POLARIZED LLC
Manufactured In: United States, Mexico
Units Affected: 18, 126 bottles
Distributed To: Nationwide

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 · 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.