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
When the arterial master pump is assigned as an intervention for the cardioplegia master pump in the hl30 version 2.0 there is a delayed stop of two seconds when the aterial master pump stops abruptly.