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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Immediately after creating a setup field in rt chart version 7.3.10 the focus reverts to the treatment field. varian has received reports that users have sometimes failed to notice this focus and have proceeded to delete mlc and other accessory components from the field in the mistaken belief they were acting on the setup field.