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 when the epiq 5 epiq 7 or affiniti 70 ultrasound systems are set up to 'metric' and weight and/or height is entered a unit conversion error may result in the incorrect calculation of the patient's body surface area (bsa).