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
If a sample is manually loaded to the access 2i and no program is at the access 2i or dxc console a program is sent by the lis only to the dxc console and the sample will not be processed at the access 2i.