Z-1807-2026 Class II Ongoing
FDA device recall Z-1807-2026 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: 480,000.
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
- 480,000
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.
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.