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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The heartstart mrx instructions for use have been improved with an addendum to better clarify the co2/etco2 measurements taken by the mrx devices with software versions f.02 r.02 9.Xx or earlier versions. the addendum describes co2/etco2 functionality when patient co2 levels drop to very low levels and what to do if such situations arise.