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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There is a risk that these electrodes will be connected with the defibrillator only with delay or not at all. this may cause a situation in which a patient who is in a life-threatening condition and requires a defibrillation shock cannot be treated in good time.