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 has received a complaint indicating that the non-gated bolus tracking clinical scan failed to initialize with the system displaying the error message "a problem has occurred- please retry. if the problem persists contact service." this resulted in the study being cancelled with a loss of bolus. if this were to re-occur it may necessitate a rescan.