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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An anomaly has been identified in the 4d structure merge optioni of certain versions of varian's eclipse treatment planning system. use of the 4d structure merge tool may result in displacement of merged contours if a couch structure was inserted prior to the merge.