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 reported that under certain circumstances when starting the system up or reconnecting the c-arm cable to the main unit the error 5000/243 "no x-ray - fd re-initializes" may occur. the error refers to a potential hardware malfunction which requires a part replacement. when this error occurs the system will become inoperable (i.E. no x-ray) until the affected part is replaced.