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 has recently determined that when certain patient monitors (mx400 mx450 mx500 and mx550) have been powered on continuously for at least three months the waveforms displayed on the monitor may be outdated and therefore fail to reflect the patient's current condition. should this occur however the monitor's alarms and numeric displays of vital signs will continue to function as specified and accurately reflect current patient data.