The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure... recall (Uvlizer c/o RAIS INTERNATIONAL LLC)
Medical deviceClass IIOngoing
Summary: Uvlizer c/o RAIS INTERNATIONAL LLC is recalling 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.
What is being recalled
The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure mercury bulbs with a peak emission wavelength at 254 nm.
Why
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.
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
U.S.
How to tell if yours is affected
None provided.
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-1807-2026 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | March 6, 2026 |
| Reported | April 29, 2026 |
| Company | Uvlizer c/o RAIS INTERNATIONAL LLC |
| Company location | Lewes, DE, United States |
| Initiated by | FDA Mandated |
| Quantity | 480,000 |
More recalls from Uvlizer c/o RAIS INTERNATIONAL LLC · all medical device recalls · recalls from March 2026