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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Anomaly within varis vers 6.2.27 and 6.1.35 involving plans created for treatment by elektra or ge machines that make use of a motorized wedge upon transfer the wedge mu field within varis may be set to zero.