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
Voluntary action to provide users with additional information regarding sterile adapter engagement and instrument installation. although rare sterile adapter and instrument engagement issues may lead to non-intuitive motion or a sluggish response when controlling instruments. these characteristics are apparent prior to interaction with tissue and thus do not pose a risk to health or safety of patients or users.