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 in a limited number fr3 aeds the printed circuit board (pcb) which contains the circuitry that supplies energy to the device could become separated from the electrical contact points that hold the board in place. in the event the pcb becomes separated from the electrical contact points the aed may not be ready to deliver a shock in the event of an emergency.