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 intellivue g5 essential gas module (egm) may display an unusually high sample flow rate up to 420ml/min instead of 200ml/min +/-20 ml/min. this high flow rate will result in a failed zero calibration and may result in additional technical alarms (inops) and in the display of a question mark <-?-> instead of a numeric value for the measured gases.