OttLite Rechargeable UVC Disinfecting Wand — Class II medical device recall Z-1473-2023
Ongoing recall by Ottlite TEchnologies, Inc., reported 2023-05-10. Product allows for the emission of ultraviolet (UV) electronic product radiation in excess of exposure limits
| Recall number | Z-1473-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | FDA mandated |
| Recalling firm | Ottlite TEchnologies, Inc., Tampa, FL, United States |
| Recall initiated | 2022-11-17 |
| Classified | 2023-05-01 |
| Reported by FDA | 2023-05-10 |
| Quantity | 7,376 units |
| Model numbers | UV10002M |
Product
OttLite Rechargeable UVC Disinfecting Wand
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1473-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.