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 if a customer creates customized trend scales in the trend review tile and the ix or primary server reboots for any reason the ix(s) will enter a reboot loop. if one ix reboots the issue will impact only those patients monitored on that device. if the primary server reboots all patients across all ix devices will be impacted.