Class II

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

Uvlizer c/o RAIS INTERNATIONAL LLC · March 6, 2026

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.

Quantity Affected

480,000

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1807-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.