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 x-ray tube / collimator became dissociated from its support causing it to fall out of position. the assembly was retained by the cables and there were no collision with the patient's support panel. the probable cause for the failure is the fragility of the welding of part m009g001 " axe support tube".