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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If 80 kvp is selected for a low dose ct on a gemini 64 pet/ct during the pet acquisition the concurrent reconstruction will fail and the customer may think that their images were lost. this may cause the customer to re-scan the patient.