Recall archive / FDA device enforcement
OttLite Rechargeable UVC Disinfecting Wand — FDA record Z-1473-2023
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 Nov 17, 2022. 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
- OttLite Rechargeable UVC Disinfecting Wand
- Reason
- Product allows for the emission of ultraviolet (UV) electronic product radiation in excess of exposure limits recommended by the International Commission on Non-ionizing Radiation Protection (ICNIRP). The emissions are hazardous to users and others in the vicinity.
- Classification
- Class II
- Recalling firm
- Ottlite TEchnologies, Inc.
- Quantity
- 7376 units
- Agency-reported status
- Ongoing
- Source record identifier
- Z-1473-2023
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 | model: UV10002M |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
US Natioonwide Distribution
No US distribution state could be established from this record. Check the official notice.
Dates in the source
- Report date
- May 10, 2023
- Recall initiation date
- Nov 17, 2022
- Center classification date
- May 1, 2023
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.