SUN|DASH RADIUS 252 tanning system — Class II medical device recall Z-2334-2012
Terminated recall by JK Products & Services, Inc, reported 2012-09-19, distributed nationwide. The firm has tracked a systematic failure in the door cord on the Sun|Dash Radius 252 product line. In some in
| Recall number | Z-2334-2012 |
|---|---|
| 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 | 2005-07-08 |
| Classified | 2012-09-07 |
| Reported by FDA | 2012-09-19 |
| Terminated | 2017-01-13 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 1,948 units |
| Serial numbers | 248-1298 |
Product
SUN|DASH RADIUS 252 tanning system; 52 lamps, Ultraviolet Radiation. The device is intended to be used for tanning of the human skin.
Reason for recall
The firm has tracked a systematic failure in the door cord on the Sun|Dash Radius 252 product line. In some instances when the door cord is installed with little or no slack outside the upper decor piece, the cord has been known to fail causing a short in the wiring at the pivot point in the cord.
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-2334-2012. 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.