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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Cardiac science has determined that the affected lot may exhibit higher than expected electrical impedance over time. if electrode impedance becomes too high the g3 aed will fail the electrode self-test performed by the aed and it will not be rescue ready.