Recall archive / FDA device enforcement
The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure mercury bulbs with a peak emiss... — FDA record Z-1807-2026
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Mar 6, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- 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.
- Classification
- Class II
- Recalling firm
- Uvlizer c/o RAIS INTERNATIONAL LLC
- Quantity
- 480,000
- Agency-reported status
- Ongoing
- Source record identifier
- Z-1807-2026
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | None provided. |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
U.S.
No US distribution state could be established from this record. Check the official notice.
Dates in the source
- Report date
- Apr 29, 2026
- Recall initiation date
- Mar 6, 2026
- Center classification date
- Apr 17, 2026
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.