FDA Device recall Z-2334-2012
SUN|DASH RADIUS 252 tanning system
- FDA Device
- Class II
- terminated
- Published 2012-09-19
On 2012-09-19 the FDA classified a Class II recall of SUN|DASH RADIUS 252 tanning system by Jk Products And Services, citing 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 outsi….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2334-2012 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2005-07-08 |
| Published | 2012-09-19 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Jk Products And Services |
| Distribution | US |
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
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.
Identifiers
| code_info | PN 8000809705; Serial numbers 248-1298 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2334-2012%22
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