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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In certain cpr meters shipped as part of the q-cpr option of the heartstart mrx monitor/defibrillator (m3535a/m3536a) the force measurement sensor in these cpr meters can gradually lose sensitivity with use. this can result in inaccurate feedback to the user on how well he or she is releasing pressure after each chest compression.