FDA Device recall Z-2635-2014
SUN DASH RADIUS 252 PN 8000809705
- FDA Device
- Class II
- terminated
- Published 2014-09-24
On 2014-09-24 the FDA classified a Class II recall of SUN DASH RADIUS 252 PN 8000809705 by Jk Products And Services, citing the integrity of the wires inside main electrical chord become compromised from excessive flexing (during the door open/close process).
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2635-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-07-25 |
| Published | 2014-09-24 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Jk Products And Services |
| Distribution | US |
Product
SUN DASH RADIUS 252 PN 8000809705. The device is intended to be used for the tanning of human skin.
Reason
The integrity of the wires inside main electrical chord become compromised from excessive flexing (during the door open/close process).
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-2635-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.