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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There is a risk that the set patient temperature in hcu 30 could randomly be changed to an incorrect value due to erroneous detection of temperature probe in the rcu 30 although no probe is connected.