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 atrium thoracic catheters are packaged with a label containing an icon that depicts that product as having multiple eyelets. the graphical icon is designed to represent a generic thoracic catheter and does not accurately reflect the actual eyelet configuration of the product contained in the package. the packaging is transparent allowing visualization of the actual number of eyelets on the thoracic catheter.