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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A software upgrade to the liaison xl analyzer activities will be conducted because the completed results in the "done" folder under the "results" tab may not be aligned properly until the software aut0-refreshes or after leaving and reentering the "done" folder.