The product is a handheld ultraviolet-C germicidal wand and contains… — Class II medical device recall Z-1807-2026
Ongoing recall by Uvlizer c/o RAIS INTERNATIONAL LLC, reported 2026-04-29. In some foreseeable use conditions, the Products can expose nearby persons to UVC radiation at levels signific
| Recall number | Z-1807-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | FDA mandated |
| Recalling firm | Uvlizer c/o RAIS INTERNATIONAL LLC, Lewes, DE, United States |
| Recall initiated | 2026-03-06 |
| Classified | 2026-04-17 |
| Reported by FDA | 2026-04-29 |
| Quantity | 480,000 |
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 for recall
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.
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-1807-2026. 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.