FDA Medical Device Recalls (openFDA)
JK Products & Services, Inc: SUN DASH RADIUS 252 PN 8000809705. The device is intended to be used for the tanning of human skin.
- Recall number
- Z-2635-2014
- Recalling firm
- JK Products & Services, Inc
- Product
- SUN DASH RADIUS 252 PN 8000809705. The device is intended to be used for the tanning of human skin.
- Status
- Terminated
- Initiated
- 2014-07-25
- Posted
- 2014-09-12
- Terminated
- 2017-01-13
- Reason
- The integrity of the wires inside main electrical chord become compromised from excessive flexing (during the door open/close process).
- Root cause
- Device Design
- Action
- The owners of the affected device will be notified via certified letter. After the recalling firm confirms ownership, a technician will be dispatched to install a door clamp and door stop, and inspect the condition of the main electrical chord.
- Quantity
- 1948 units
- Distribution
- Nationwide Distribution.
- Lot, serial or model codes
- PN 8000809705; Serial numbers 248-1298
- 510(k) numbers
- ["K932483"]
- PMA numbers
- not on file
- Product code
- LEJ
- Firm FEI
- 2311923
- Firm city
- Jonesboro
- Firm state
- AR
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28