UVT INC recalls Saniderm ADVANCED HAND SANITIZER, 70% Alcohol Content, 1 Liter bottles, Distributed by Polarized, LLC, Produced by
UVT INC recalls Saniderm Advanced Hand Sanitizer (1L) due to undeclared methanol. Consumers should stop using affected products to avoid chemical contamination risks.
Stop using this now
Chemical Contamination: Product contains undeclared methanol.
Contact the company & request your remedy
What happened, in plain English
UVT INC is recalling Sanider: 70% alcohol hand sanitizer bottles because they contain undeclared methanol. This chemical contamination could cause health risks if ingested or absorbed through skin. Read more at govinfonow.com/recall/37005-uvt-saniderm-hand-sanitizer-recall-methanol-contamination-hazard.
Source Summary by GovInfoNow · govinfonow.com/recall/37005-uvt-saniderm-hand-sanitizer-recall-methanol-contamination-hazard · Updated October 5, 2026 · FDA enforcement record: FDA #D-1407-2020
Cite this page
“UVT Saniderm Hand Sanitizer Recall: Methanol Contamination Hazard.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37005-uvt-saniderm-hand-sanitizer-recall-methanol-contamination-hazard. Based on FDA recall #D-1407-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1407-2020%22&limit=1).
Why it’s dangerous
Methanol is a toxic alcohol that can cause serious health issues if absorbed through skin or ingested. In hand sanitizers, methanol can lead to poisoning, vision damage, or organ failure if not properly regulated.
Who’s affected
Anyone who owns the Saniderm Advanced Hand Sanitizer 1L bottles with lot number 0530 or expired by April 2022. Children and people with sensitive skin are at higher risk due to methanol exposure.
How to tell if you have this one
Check for Saniderm Advanced Hand Sanitizer 1L bottles with lot number 0530 or expiration date of April 2022. The product was distributed by Polarized, LLC and produced in Mexico.
- Brand
UVT INC- Product
Saniderm ADVANCED HAND SANITIZER, 70% Alcohol Content, 1 Liter bottles, Distributed by Polarized, LLC, Produced by- Category
Drug
What to do — step by step
Stop Using Now
Immediately stop using the recalled Saniderm Advanced Hand Sanitizer bottles to avoid potential methanol exposure.
Questions people ask
Is this product safe to use?
No, the product contains undeclared methanol which poses a health risk. Do not use the recalled bottles.
How can I check if my product is recalled?
Look for Saniderm Advanced Hand Sanitizer 1L bottles with lot number 0530 or expiration date of April 2022.
What should I do with the recalled product?
Discard the product immediately as it contains undeclared methanol that could cause health risks.
Contact UVT INC
We’ve drafted a message you can send UVT INC to request your refund or repair — edit it as you like.
Subject: Recall D-1407-2020 — UVT INC Saniderm ADVANCED HAND SANITIZER, 70% Alcohol Content, 1 Liter bottles, Distributed by Pola Hello, I own a Saniderm ADVANCED HAND SANITIZER, 70% Alcohol Content, 1 Liter bottles, Distributed by Polarized, LLC, Produced by that is covered by recall D-1407-2020 from UVT INC. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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-1407-2020 (June 22, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1407-2020 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.