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
334
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 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.
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.