CLASS II Device recall · Reported 24 Sep 2014 · FDA Enforcement Report
Sun Dash Radius 252 Pn recalled by JK Products & Services
JK Products & Services is recalling Sun Dash Radius 252 Pn 8000809705, distributed nationwide in the US. The recall was initiated on 25 Jul 2014 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-2635-2014
- FDA event ID
- 69038
- Recalling firm
- JK Products & Services, Jonesboro, AR
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 25 Jul 2014
- FDA classified
- 12 Sep 2014
- Reported
- 24 Sep 2014
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 25 Jul 2014 | Recall initiated by company | |
| 12 Sep 2014 | Classified by FDA | +49 days |
| 24 Sep 2014 | 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 integrity of the wires inside main electrical chord become compromised from excessive flexing (during the door open/close process).
Product as listed by the FDA
SUN DASH RADIUS 252 PN 8000809705. The device is intended to be used for the tanning of human skin.
Where it was distributed
Nationwide Distribution.
Questions about this recall
Is Sun Dash Radius 252 Pn 8000809705 recalled?
Yes. JK Products & Services recalled Sun Dash Radius 252 Pn 8000809705 on 25 Jul 2014. The recall is Class II and its status is Terminated. Recall number Z-2635-2014.
Why was it recalled?
The integrity of the wires inside main electrical chord become compromised from excessive flexing (during the door open/close process).
Which lots are affected?
PN 8000809705; Serial numbers 248-1298
Where was it sold?
Nationwide Distribution.
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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