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
Defectuosite trouvee dans la mesure de o2 cause par un eprom u42 qui n'indiquerait pas une erreur du zero de o2 si le capteur de o2 devient defectueux. pourrait afficher mesures de o2 erronees.