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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In certain external transport use environments the mechanical/electrical connection between the pads therapy cable (including pads/cpr cable) and the heartstart mrx defibrillator/monitor may wear at an increased rate. without routine operational checks wear of the connection could ultimately prevent the device from sensing that the pads therapy cable is connected or cause the device to inappropriately identify external paddles or internal paddles when the pads therapy cable is connected.