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
There may be an occlusion in the catheter which precludes the catheter from draining excessive pleural fluid from the pleural cavity during a thoracentesis procedure. this occlusion could potentially cause a delay in the procedure leading to serious patient complications and a potential patient safety risk.