Recall Z-2334-2012— JK Products & Services, Inc
Class II · Terminated
Class II FDA medical device recall by JK Products & Services, Inc, initiated 2005-07-08, terminated 2017-01-13. FDA's recall record names no specific 510(k) clearance for this event. 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..
- Recalling firm
- JK Products & Services, Inc
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2005-07-08
- Terminated
- 2017-01-13
- Firm location
- Jonesboro, AR, United States
Product description
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.