Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

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.

ยฉ 2026 Go Backs. All rights reserved.

Critical RiskFDA Drug
Medications & Supplements/Topical Products

UVT INC: Saniderm Advanced Hand Sanitizer Recalled for Undeclared Methanol

Agency Publication Date: July 24, 2020
Share:
Sign in to monitor this recall

Summary

UVT INC is recalling approximately 38,016 bottles of Saniderm Advanced Hand Sanitizer (70% alcohol content) because the product contains undeclared methanol, also known as wood alcohol. These 1-liter bottles were distributed to wholesalers in Florida and may have been sold nationwide. Consumers who have this hand sanitizer should immediately stop using it and contact their healthcare provider or pharmacist, as methanol is not an acceptable ingredient for hand sanitizers and can be toxic if absorbed through the skin or ingested.

Risk

Methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system, or death. While anyone using these products on their hands is at risk, young children who accidentally ingest them and adolescents or adults who drink them as an alcohol substitute are at highest risk for methanol poisoning.

What You Should Do

  1. Check your hand sanitizer bottles for the brand name 'Saniderm ADVANCED HAND SANITIZER' in 1-liter (1000ml) bottles.
  2. Verify the product identification by looking for UPC 8 60003 63391 5 and Lot Number 0530 with an expiration date of 04/22.
  3. Immediately stop using the product if it matches the recalled lot and UPC information.
  4. Contact your healthcare provider or pharmacist for guidance if you have experienced any health problems that may be related to using this hand sanitizer.
  5. Return any unused product to the pharmacy or place of purchase for a refund and contact UVT INC at 5000 Birch St, Ste. 3000, Newport Beach, California for further instructions.
  6. For additional information or to report a reaction, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

๐Ÿ’ฐFull Refund

Drug Recall Remedy

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)
UPC Codes:
860003633915
Lot Numbers:
0530 (Exp. Date 04/22)
Date Ranges: Expiration Date 04/22

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 85942
Status: Resolved
Manufacturer: UVT INC
Sold By: wholesalers
Manufactured In: Mexico, United States
Units Affected: 38,016 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 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.