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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When the imaging system is running for a long period of time without interruption it might occur in rare cases that images are not stored correctly. in this case the imaging system would have to be restarted and the examination would have to be repeated leading to increased examination time and additional radiation dose for patient.