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 a reject image workflow where multiple studies are simultaenously opened on the centricity pacs ra1000 workstation and images are rejected from the active displayed study images from the previously displayed study may also be rejected. the issue can occur with a previously displayed study that remains open in the background.