FDA Recall
Open, Classified
The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure mercury bulbs with a peak emission wavelength at 254 nm.
Recall: Z-1807-2026
·
Initiated March 6, 2026
Recall
- Recall Number
- Z-1807-2026
- Event Number
- 98747
- Firm
- Uvlizer c/o RAIS INTERNATIONAL LLC
- FEI Number
- 3031733296
- Product Code
- RHP
- Status
- Open, Classified
- Root Cause
- Radiation Control for Health and Safety Act
- Initiated
- March 6, 2026
- Posted
- April 17, 2026
- Address
- 16192 Coastal Hwy, Lewes, DE, 19958-3608
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
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.
Action
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.
Distribution
U.S.
Quantity
480,000