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
The recall is due to the posibility to have one patient selected in the patient list of nicvue and have a different patient's exams shown in the nicvue exam list. in this situation you can open an exam from the exam list that does not match the patient selected in the patient list.