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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Spacelabs has received multiple complaints reporting an abnormally high frequency of "squelch" events on xhibit telemetry receivers (xtr) which is indicative of the loss of the telemetry data signal. in some cases the xhibit central monitor was also reported to display an "xhibit offline" error message for all patients being monitored. no one has been injured due to this issue.