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.
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A potential problem with loose encoder pulleys in the imaging arms of the truebeam accelerator has been found. to date one loose encoder pulley for the wrist has been detected in a clinically operating truebeam accelerator. the problem was identified during arm initialization and the geometric error would have been ~0.5mm. importantly loose encoder pulleys can be detected by daily checks of imager arm geometry.