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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Philips healthcare received a report from the field about an adac vertex plus system. during clinical use in the relative 180 degree configuration of the detector heads the radius drive belt in the superior positioned head slipped off the idler pulley allowing the detector head to drift down slowly (approximately 1cm per minute) towards the patient. this resulted in the operator having to perform an emergency removal or the patient from the system.