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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Heartstart hs1 and frx automated external defibrillators (aeds) manufactured in march 2010 contain a relay that may not meet philips performance standards. possible contamination on the relay surface could compromise its performance over time and affect the aed's ability to make a therapy decision during use.