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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 Device
Medical Devices/Home Healthcare

Uvlizer Handheld UVC Germicidal Wands Recalled for Excessive Radiation Risk

Agency Publication Date: April 17, 2026
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Summary

RAIS INTERNATIONAL LLC is recalling 334 Uvlizer handheld ultraviolet-C (UVC) germicidal wands because they can emit radiation at levels significantly above international safety guidelines. These wands contain a combination of five UV-A and UV-C LED lights and were distributed throughout the United States. No incidents or injuries have been reported to date, but the FDA has mandated this recall to prevent potential harm to users. Consumers should stop using the device immediately and contact the manufacturer or their distributor to arrange for a return, replacement, or correction.

Risk

The wands can expose the skin and eyes of the user or nearby persons to dangerous levels of UVC radiation during normal use. This exposure can cause serious injury to the skin and eyes, exceeding recommended safety limits for radiation exposure.

What You Should Do

  1. Stop using the recalled Uvlizer handheld UVC germicidal wand immediately.
  2. Identify your product by checking the LED configuration: it will have five total lights in combinations of either 1 UVC/4 UVA LEDs or 2 UVC/3 UVA LEDs, with emission wavelengths at 274 nm and 397 nm.
  3. Contact Uvlizer c/o RAIS INTERNATIONAL LLC or your distributor to arrange for the return, replacement, or correction of the device.
  4. Call the FDA Consumer Complaint hotline at 1-888-463-6332 for additional questions regarding this mandated recall.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: Uvlizer Handheld UVC Germicidal Wand
Variants: 1 UV-C and 4 UV-A LEDs, 2 UV-C and 3 UV-A LEDs

Peak emission wavelengths at 274 nm and 397 nm.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98742
Status: Active
Manufacturer: Uvlizer c/o RAIS INTERNATIONAL LLC
Sold By: Uvlizer
Manufactured In: United States
Units Affected: 334
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.