Z-1808-2026 Class II Ongoing
FDA device recall Z-1808-2026 was initiated by Uvlizer c/o RAIS INTERNATIONAL LLC on March 6, 2026 and is designated Class II. 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 expos… The recall status is ongoing. Affected quantity: 334.
Recall Details
- Product Type
- Devices
- Report Date
- April 29, 2026
- Initiation Date
- March 6, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- FDA Mandated
- Product Quantity
- 334
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.
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 Pattern
U.S.
Code Information
None provided.