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
Collisions and excessive force exerted on the lower portion of the detector arms of the skylight spect systems may have resulted in the detector arms breaking. a collision or excessive force may lead to a crack or fracture in the upper portion of the arm which may cause the detector arms to break and the arm and detector to fall.