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 using the intellivue clinical information portfolio edits to a scheduled even frequency order may result in pending interventions not being generated after the first 24 hours. if the clinical team is solely relying on the icip critical care worklist for administration of pending orders this issue may result in a patient not receiving intended treatment.