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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Siemens is informing customers via a customer advisory letter that their biograph mct or mct flow system (with petsyngo vg40x or vg50a software installed) could experience an intermittent pet attenuation corrected image artifact which may impact the ability to obtain reliable data from the resulting image.