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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The autospect pro application was only designed to reconstruct cardiac spect data obtained with detectors positioned at 90? or 180? relative to one another. however certain gamma cameras e.G. the marconi axis and irix cameras permit acquisitions at other relative detector angles. philips has become aware that data acquired at these other angles will not be correctly reconstructed by autospect pro and the results will likely be erroneous.