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 table shift in the vertical direction was inverted during treatment. an inverse shift will result in the patient being out of position by double the shift magnitude. a mac file is instrumental to the correct operation if values are incorrectly input inverse shifts may occur.