Germicidal wand Recall: Uvlizer RAIS INTERNATIONAL
Announced 2026-04-29 · FDA
The product is a handheld ultraviolet-C germicidal wand containing two low-pressure mercury bulbs with a peak emission of 254 nm. In some foreseeable use conditions, it can expose nearby persons to UVC radiation at levels significantly above safety guidelines for skin and eye exposure. About 480,000 units were distributed in the United States, and the FDA is the involved agency; no recall number is provided.
| Brand | Uvlizer c/o RAIS INTERNATIONAL LLC |
|---|---|
| Product | 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. |
| Severity | moderate |
| Units affected | 334 |
| Distribution | U.S. |
| Agency | FDA |
| Recall / campaign no. | None provided. |
WHAT YOU SHOULD DO
- Stop using the wand immediately and keep it away from people.
- Check if you own the product and follow FDA guidance for updates.
- Contact the distributor for disposal or return instructions.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.