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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During bed exposures in a 90 degree tilted table position and a tube arm swing of 90 degrees the tube arm may be moved down to a critical position where it can collide with the patient bed or others.