Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
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Elekta has identified that if the microswitch within the pcb assembly solenoid limit switch of the middle arm is incorrectly setup there is a potential for an uncontrolled extention of iviewgt / xvi detector arms.