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 become aware that while performing high resolution head scans the reconstructed images may exhibit degraded image quality manifested as: - non uniformity of the image - ct number shift greater than 5 hounsfield units - reduction in gray/white matter differentiation the issue is most severe in the high resolution mode. philips provides factory reference pediatric scan protocols which are set to high resolution by default. adult head scans have a factory reference protocol that defaults to standard resolution which does not experience the issue.