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 the installed x-ray warning label at the digitaldiagnost with software release 4.0.X/4.1.X (eeca) is not in accordance with the local canadian regulations. a statement prohibiting unauthorized use and warning that hazardous x-rays are emitted when the equipment is in operation and the x-ray warning symbol as required under the radiation emitting devices regulations are missing.