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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There is the possibility that during stitching on the table a failure occurs and the last single image is not available. in this case a retake is necessary. there is the possibility that line artefacts will be visible at the edge of the x-ray image when using the skyplate detector.