Recalling firm
Uvlizer c/o RAIS INTERNATIONAL LLC
Product type
Device
Status
Ongoing
Report date
2026-04-29
Distribution
U.S.
Firm state
DE
Product quantity
480,000
Initiated by
FDA Mandated
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.
Product description
The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure mercury bulbs with a peak emission wavelength at 254 nm.
Code / lot info
None provided.
Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.