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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Certain heartstart fr2+ automated external defibrillators (aeds) may contain a component called a voltage detector that may have a higher than expected rate of failure. failure of the voltage detector can cause the aed battery to drain more rapidly than normal or to render the aed unusable.