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.

Class II

Recalling firm: Uvlizer c/o RAIS INTERNATIONAL LLC
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.
Affected products (lot / model / serial): None provided.
Units affected: 334
Distribution pattern: U.S.
Firm location: Lewes, DE, United States
Recall type: FDA Mandated
How the firm notified customers: N/A
Product type: Devices
Status: Ongoing
Recall number: Z-1808-2026
Recall initiated: March 6, 2026
FDA classification date: April 17, 2026
FDA report date: April 29, 2026
FDA event ID: 98742
Last updated on HTM Vibe: July 24, 2026