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
During examination if the patient is positioned with his knees pointed to the rear of the system and the operator performs a wrong movement of the scanning beam downwards instead of upwards the leg(s) of the patient might collide with the stand and get squeezed potentially resulting in a (serious) injury.