SUN DASH RADIUS 252 PN 8000809705 — Class II medical device recall Z-2635-2014
Terminated recall by JK Products & Services, Inc, reported 2014-09-24, distributed nationwide. The integrity of the wires inside main electrical chord become compromised from excessive flexing (during the
| Recall number | Z-2635-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | JK Products & Services, Inc, Jonesboro, AR, United States |
| Recall initiated | 2014-07-25 |
| Classified | 2014-09-12 |
| Reported by FDA | 2014-09-24 |
| Terminated | 2017-01-13 |
| Distributed | Nationwide (US) |
| Quantity | 1,948 units |
| Serial numbers | 248-1298 |
Product
SUN DASH RADIUS 252 PN 8000809705. The device is intended to be used for the tanning of human skin.
Reason for recall
The integrity of the wires inside main electrical chord become compromised from excessive flexing (during the door open/close process).
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-2635-2014. 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.