CLASS II Device recall · Reported 19 Sep 2012 · FDA Enforcement Report
Sun|Dash Radius 252 tanning system recalled by JK Products & Services
JK Products & Services is recalling Sun|Dash Radius 252 tanning system, distributed nationwide in the US. The recall was initiated on 8 Jul 2005 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-2334-2012
- FDA event ID
- 61869
- Recalling firm
- JK Products & Services, Jonesboro, AR
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 8 Jul 2005
- FDA classified
- 7 Sep 2012
- Reported
- 19 Sep 2012
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Device Malfunction
- Device type
- Other Medical Devices
Timeline
| 8 Jul 2005 | Recall initiated by company | |
| 7 Sep 2012 | Classified by FDA | +2618 days |
| 19 Sep 2012 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
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.
Device recalls are issued when a component, software or design fault could cause the device to fail or give wrong readings. Many are corrections applied in the field rather than physical returns.
Product as listed by the FDA
SUN|DASH RADIUS 252 tanning system; 52 lamps, Ultraviolet Radiation. The device is intended to be used for tanning of the human skin.
Where it was distributed
Worldwide Distribution - USA (nationwide) and Canada
Questions about this recall
Is Sun|Dash Radius 252 tanning system recalled?
Yes. JK Products & Services recalled Sun|Dash Radius 252 tanning system on 8 Jul 2005. The recall is Class II and its status is Terminated. Recall number Z-2334-2012.
Why was it recalled?
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.
Which lots are affected?
PN 8000809705; Serial numbers 248-1298
Where was it sold?
Worldwide Distribution - USA (nationwide) and Canada
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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