FDA recall Z-1807-2026

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

Product

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.

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-1807-2026