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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The hand switch to release a x-ray image at the patient table is equipped with a cable extension inside the table. a problem may occur if the connection between cable connection and hand switch is contaminated with an extraordinary large amount of fluid. in a worst case situation uncontrolled release of a x-ray image may happen. if this situation occurs the system terminates uncontrolled x-ray after a short period.