The product is a handheld ultraviolet-C germicidal wand and contains… — Class II medical device recall Z-0457-2023
Ongoing recall by PHONESOAP, reported 2022-12-28, distributed nationwide. Excessive ultraviolet-C radiation
| Recall number | Z-0457-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | FDA mandated |
| Recalling firm | PHONESOAP, Provo, UT, United States |
| Recall initiated | 2022-08-30 |
| Classified | 2022-12-16 |
| Reported by FDA | 2022-12-28 |
| Distributed | Nationwide (US) |
| Quantity | 6,700 systems |
Product
The product is a handheld ultraviolet-C germicidal wand and contains narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range.
Reason for recall
Excessive ultraviolet-C radiation
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-0457-2023. 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.