Home / Recalls / Medical Devices
JK Products & Services, Inc recalls SUN DASH RADIUS 252 PN 8000809705. The device is intended to be used for the tanning of human skin.
Recalled September 24, 2014 · FDA recall Z-2635-2014 · JK Products & Services
Hazard
The integrity of the wires inside main electrical chord become compromised from excessive flexing (during the door open/close process). · FDA Class II
Units
1948 units
Sold at
Nationwide Distribution.
Description
The integrity of the wires inside main electrical chord become compromised from excessive flexing (during the door open/close process).
Product
SUN DASH RADIUS 252 PN 8000809705. The device is intended to be used for the tanning of human skin.
Manufacturer(s)
JK Products & Services, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →