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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Areas that should receive no dose may be treated and areas that are supposed to be treated may receive more or less dose than they should. the dicom exported plan and subsequent treatment delivery will not match the approved treatment plan. there is a remote probability of the issue resulting in serious adverse health consequences.