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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During routine operations the detectors housing is manipulated for best positioning. if the detector head is pulled or pushed aggressively and repeatedly this type of handling might result in extreme cases the detector head to slide out from the gantry. in this case possible damage to the system or contacting with patient's legs might occur.