FDA DevicesClass II
The product is a handheld ultraviolet-C germicidal wand and contains a combinati...
Published: April 29, 2026Recall ID: Z-1808-2026Category: 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 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.
Additional Source Details
| Field | Value |
|---|---|
| City | Lewes |
| State | DE |
| Event id | 98742 |
| 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 | 334 |
| 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.