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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It has been found that when the c-arm is switched from pa mode to ap mode using the auto positioning button under certain specified conditions the c-arm may interfere with the tabletop due to a problem in the firmware.