FDA recall Z-1808-2026

Uvlizer c/o RAIS INTERNATIONAL LLC · Class II · device

Product

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

U.S.

Key facts

Status
Ongoing
Initiation date
2026-03-06
Report date
2026-04-29
Voluntary/Mandated
FDA Mandated
Location
Lewes, DE, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1808-2026