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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Some heartstart frx automated external defibrillators (aeds) model 861304 contain a high voltage (hv) capacitor from a lot that does not meet philips' quality standards. if the aed has an hv capacitor exhibiting low capacitance or a high dissipation factor the device may be unable to deliver the appropriate therapy.