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
In january 2016 a customer complaint reported a mismatch between the prescribed dose value displayed on the screen and the prescribed dose value printed by the printer. the dose activity infused was as intended and printed correctly.