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 users may have assumed that the spo2 non-pulsatile and spo2 no sensor technical alarms were enabled when the suresigns vs3 vital signs monitor was not in interval non-invasive blood pressure (nbp) mode.