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-1808-2026Medical 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 a combination of five UV-A and UV-C LED lights. The product comes in two configurations: UV-C x 1; UV-A x 4, or UV-C x 2; UV-A x 3. The product has two peak emission wavelengths at 274 nm and 397 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
The FDA classified this recall as Class II, indicating the medical device may cause temporary health problems or poses a slight threat of a serious nature. Uvlizer c/o RAIS INTERNATIONAL LLC initiated the recall on March 6, 2026 affecting 334. 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. The product was distributed in U.S. Consumers should check their purchases and discontinue use of any affected product. Contact Uvlizer c/o RAIS INTERNATIONAL LLC for further instructions.
Sources: FDA openFDA Enforcement Database
This recall appears in: Other Injury Hazards.