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
An anomaly has been identified when using the 4ditc in combination with a retractable arm (r - arm) to acquire double exposure mv images. when using a very specific image acquisition process the field outline is incorrectly copied from the treatment port image to the open port image. if the field outline from the treatment port image is then used to adjust the "imager position correction" in offline review the digitally reconstructed radiograph (drr or reference image) and any superimposed contours will be displaced incorrectly because of the incorrect placement of the detected field edge.