Uvlizer c/o RAIS INTERNATIONAL LLC recalls The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure mercury bulbs with a peak emissio…

Recall date

March 6, 2026

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-1807-2026

FDA classification

Class II

Brand / firm

Uvlizer c/o RAIS INTERNATIONAL LLC

Sold / distributed

U.S.

Why it was recalled

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure mercury bulbs with a peak emission wavelength at 254 nm.