FDA DevicesClass II
The product is a handheld ultraviolet-C germicidal wand and contains two low-pre...
Published: April 29, 2026Recall ID: Z-1807-2026Category: devicesCountry: US
Reason for Recall / 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.
Product Description & Identification
The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure mercury bulbs with a peak emission wavelength at 254 nm.
Additional Source Details
| Field | Value |
|---|---|
| City | Lewes |
| State | DE |
| Event id | 98747 |
| Address 1 | 16192 Coastal Hwy |
| Address 2 | N/A |
| Code info | None provided. |
| Postal code | 19958-3608 |
| Report date | 20260429 |
| Product type | Devices |
| Product quantity | 480,000 |
| 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. |
| Voluntary mandated | FDA Mandated |
| Recall initiation date | 20260306 |
| Initial firm notification | N/A |
| Center classification date | 20260417 |
Overview
- Recalling FirmUvlizer c/o RAIS INTERNATIONAL LLC
- StatusOngoing
- Risk LevelClass II
- DistributionU.S.