Official recall notice
FDA DeviceClass IINotable
FDA Recall: The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure mercury bulbs
- Recall date
- 2026-04-29
- Category
- Medical Device
- FDA class
- Class II
Why it was recalled
Hazard
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.
Recommended action
What to do
480,000
Product description
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.