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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Philips healthcare has become aware that the heartstart mrx monitor/defibrillator devices may fail to deliver defibrillation therapy in either manual defib or aed mode. if this occurs the mrx may simultaneously display a "no shock delivered" message along with a "shock equip malfunction" inop and a red x in the rfu indicator. in addition the pads ecg waveform may display a non-physiologic flat line rhythm.