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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Potential hazard associated with the use of all patient monitors equipped with the perioperative option (-d). operating room staff may not be aware that alarm tones are off if the device has been left in the end case state. this is more likely to occur in emergency surgery situations and with surgical teams that are not familiar with the monitor's operation.