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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 Device
Medical Devices/Home Healthcare

Uvlizer Germicidal Wand Recalled for Excessive UVC Radiation Risk

Agency Publication Date: April 17, 2026
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Summary

Uvlizer c/o RAIS INTERNATIONAL LLC is recalling approximately 480,000 handheld ultraviolet-C (UVC) germicidal wands because they can emit dangerous levels of radiation. These handheld devices contain two mercury bulbs intended to kill germs, but they lack sufficient safety features to protect users. No injuries have been reported at this time, but the FDA has mandated this recall due to the severity of the radiation exposure. If you own this product, you should stop using it immediately and contact the manufacturer or your healthcare provider.

Risk

The wands expose people to UVC radiation levels significantly higher than international safety limits, which can cause severe skin burns and eye injuries within seconds of exposure.

What You Should Do

  1. Stop using the Uvlizer Germicidal Wand immediately.
  2. Identify your product by checking if it is a handheld wand containing two low-pressure mercury bulbs with a peak emission wavelength of 254 nm.
  3. Return the product to the place of purchase for a refund or replacement, throw it away, or contact your healthcare provider or Uvlizer c/o RAIS INTERNATIONAL LLC for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-463-6332 (1-888-INFO-FDA) for additional questions or to report an injury.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider, or return the product to the place of purchase for a refund or replacement
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Stop using and throw the product away.

Affected Products

Product: Uvlizer Germicidal Wand

Product contains two low-pressure mercury bulbs with a peak emission wavelength at 254 nm.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98747
Status: Active
Manufacturer: Uvlizer c/o RAIS INTERNATIONAL LLC
Sold By: Uvlizer
Manufactured In: United States
Units Affected: 480,000
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.