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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When the local configuration setting 'alarms on' is modified from its factory default in certain software revisions the philips intellivue mx40 patient wearable monitor will disable generation and delivery of ecg alarms to the philips intellivue information center ix (piic ix) without visual indication on the piic ix that the ecg alarms have been disabled. this could lead to a delay in treatment.