Uvlizer C/O RAIS INTERNATIONAL LLC recalls The product is a handheld ultraviolet-C germicidal wand and contains a combination of f…

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.

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.

Notifications to purchasers and subsequent transferees will be transmitted through multiple communication channels: Certified Mail, Email Notifications, and Public Website Notice, describing the defect, safety considerations, and instructions to discontinue use of the Product.

• FDA enforcement recordOfficial FDA database entry for Z-1808-2026
• FDA device classification · RHPOfficial FDA classification for this device type
• FDA recall announcementSearch FDA.gov for the official press announcement
• Find Uvlizer c/o RAIS INTERNATIONAL LLCSearch for the manufacturer's official notice
• News coverageRecent reporting on this recall and manufacturer
• openFDA data recordThe raw JSON record this page is built from

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.