FDA Medical Device Recalls (openFDA)
JK Products & Services, Inc: SUN|DASH RADIUS 252 tanning system; 52 lamps, Ultraviolet Radiation. The device is intended to be used for tanning of the human skin.
- Recall number
- Z-2334-2012
- Recalling firm
- JK Products & Services, Inc
- Product
- SUN|DASH RADIUS 252 tanning system; 52 lamps, Ultraviolet Radiation. The device is intended to be used for tanning of the human skin.
- Status
- Terminated
- Initiated
- 2005-07-08
- Posted
- 2012-09-07
- Terminated
- 2017-01-13
- 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.
- Root cause
- Equipment maintenance
- Action
- JK Global Services sent out Mandatory Inspection/Modification letters to their Distribution Service Teams dated 07/08/2005, 01/12/2006, 09/15/2010, 10/04/2010 and 03/01/2012. A letter dated September 15, 2010, was sent to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were asked to contact a JK representative or their Distributor as soon as possible to schedule an inspection to the affected product in their possession. For any questions customers were instructed to call 1-800-445-0624 or send an e-mail to support@jkamerica.com.
- Quantity
- 1948 units
- Distribution
- Worldwide Distribution - USA (nationwide) and Canada
- Lot, serial or model codes
- PN 8000809705; Serial numbers 248-1298
- 510(k) numbers
- not on file
- 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