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 certain oximetry modules may have been incorrectly assembled. the effect on performance when these wires are crossed is that when a low spo2 value is measured a high spo2 value would be displayed on the monitoring device. additionally in the same oximetry cable when a high spo2 value is measured a low spo2 value would be displayed on the monitoring device.