Recall Z-2635-2014— JK Products & Services, Inc
Class II · Terminated
Class II FDA medical device recall by JK Products & Services, Inc, initiated 2014-07-25, terminated 2017-01-13. It names one FDA 510(k) clearance: K932483. Product: SUN DASH RADIUS 252 PN 8000809705. The device is intended to be used for the tanning of human skin.. Reason: The integrity of the wires inside main electrical chord become compromised from excessive flexing (during the door open/close process)..
- Recalling firm
- JK Products & Services, Inc
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2014-07-25
- Terminated
- 2017-01-13
- Firm location
- Jonesboro, AR, United States
510(k) clearances named in this recall
1 on FDA's recordK-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.
Product description
SUN DASH RADIUS 252 PN 8000809705. The device is intended to be used for the tanning of human skin.
Reason for recall
The integrity of the wires inside main electrical chord become compromised from excessive flexing (during the door open/close process).
Data sourced from openFDA. This site is unofficial and independent of the FDA.