Z-2635-2014 Class II Terminated
FDA device recall Z-2635-2014 was initiated by JK Products & Services, Inc on July 25, 2014 and is designated Class II. Reason for recall: The integrity of the wires inside main electrical chord become compromised from excessive flexing (during the door open/close process). The recall status is terminated (terminated January 13, 2017). Affected quantity: 1948 units.
Recall Details
- Product Type
- Devices
- Report Date
- September 24, 2014
- Initiation Date
- July 25, 2014
- Termination Date
- January 13, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1948 units
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).
Distribution Pattern
Nationwide Distribution.
Code Information
PN 8000809705; Serial numbers 248-1298