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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In case of an ysio with fixed detector in the wall stand an unlikely error may occur resulting in line artifacts in the image. should these artifacts appear in the region of interest the examination may need to be repeated.