Z-1808-2026 Class II Ongoing

Recalled by Uvlizer c/o RAIS INTERNATIONAL LLC — Lewes, DE

Recall Details

Product Type
Devices
Report Date
April 29, 2026
Initiation Date
March 6, 2026
Termination Date
N/A
Voluntary/Mandated
FDA Mandated
Product Quantity
334

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.

Distribution Pattern

U.S.

Code Information

None provided.