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.
데이터 추가 비고
원인
Software issue in corvus 5.0 and 5.0m relative to plans created for the elekta mlc. under certain circumstances corvus does not correctly account for leakage dose from the elekta mlc.