Handheld UV-C germicidal wand recalls for excessive radiation exposure
Uvlizer handheld UV-C germicidal wands may expose users and nearby people to ultraviolet radiation at levels above international safety guidelines for skin and eye protection.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: This is an FDA Class II recall for a risk-of-harm product (excessive UV-C radiation exposure to skin and eyes) where the source explicitly states no illnesses or injuries have been reported. Per the rubric, such cases merit a High (3) rating.
Plain-English summary
Uvlizer, manufactured by RAIS INTERNATIONAL LLC, is recalling handheld ultraviolet-C germicidal wands sold in the United States. The product contains five LED lights in two configurations: UV-C x 1 with UV-A x 4, or UV-C x 2 with UV-A x 3, with peak emission wavelengths at 274 nm and 397 nm. A total of 334 units have been distributed.
Under some foreseeable use conditions, these wands can expose nearby persons to UVC radiation at levels significantly above the limits recommended by international safety guidelines for skin and eye exposure. Consumers who own this product should discontinue use and contact the manufacturer for further instructions.
The recalled product
- Product
- 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.
- Manufacturer
- Uvlizer c/o RAIS INTERNATIONAL LLC
- Hazard
- uv-c-radiation
- eye-exposure
- skin-exposure
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- None provided.
Distribution
Distribution scope not specified by the agency.
Related recalls
Same category
- ModerateSilastic Brand Foley Catheters recalled due to surface stain
FDA (Devices) · 2026-05-27
- HighIntegris-Allura X-ray systems with degraded deaeration hoses recalled
FDA (Devices) · 2026-05-27
- HighMedtronic DLP Retrograde Cannula 15FR Model 94665 Sterile Barrier
FDA (Devices) · 2026-05-27
- SevereMedtronic DLP Retrograde Cannula Recalls for Sterile Barrier Breach Risk
FDA (Devices) · 2026-05-27
- HighPhilips Azurion X-Ray Systems Table Movement Control Defect Recall
FDA (Devices) · 2026-05-27