Warning
Uvlizer c/o RAIS INTERNATIONAL LLC Recalls The product is a handheld ultraviolet-C germicidal wand
This is a Class II recall. This product may cause temporary health problems or pose a slight threat of a serious nature.
Source: FDA
WarningRecall #Z-1807-2026Medical Device
Uvlizer c/o RAIS INTERNATIONAL LLC Recalls The product is a handheld ultraviolet-C germicidal wand
Uvlizer c/o RAIS INTERNATIONAL LLC · Class II — Moderate Risk
Product Description
The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure mercury bulbs with a peak emission wavelength at 254 nm.
Reason for Recall
In some foreseeable use conditions, the Products can expose nearby persons to UVC radiation at levels significantly above limits recommended by international safety guidelines for skin and eye exposure.
FDA Classification
Class II — Moderate Risk
A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Distribution
U.S.
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
A Class II FDA recall has been issued for a medical device from Uvlizer c/o RAIS INTERNATIONAL LLC, initiated on March 6, 2026. In some foreseeable use conditions, the Products can expose nearby persons to UVC radiation at levels significantly above limits recommended by international safety guidelines for skin and eye exposure. This recall covers 480,000, distributed in U.S. While not the highest severity, consumers should exercise caution and stop using the product until the recall is resolved.
Sources: FDA openFDA Enforcement Database
This recall appears in: Other Injury Hazards.