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
On februray 14 2017 southmedic received a customer complaint indicating potential occlusion of the co2 sampling line on a southmedic capnography mask (hc recakk # 141724). after further investigation southmedic is extending the recall to include 4 product codes of the nasal cannula with co2 sampling lines.