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 become aware that the spo2 and non-invasive blood pressure (nibp) waveform and numeric values displayed on the device may freeze resulting in the display of measurements that are not current. although spo2 and nibp monitoring and alarms are no longer functional all other monitoring parameters are functional and visible. if this problem were to occur the device can be reset by power cycling and the reset will allow the customer to continue monitoring. however power cycling the device does not prevent the issue from recurring.