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
Siemens has become aware that some light marker windows on biograph mct and biograph mct flow systems may loosen and potentially drop out. in this case there is a risk that a person could touch the electrical or rotating parts of the gantry were they to reach through the window opening.