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 pdm patient parameter acquisition module can somtimes spontaneously lose the communication with the host patient monitor when attached to the f5-01 frame of the carescape monitor b850 due to an issue with the pdm ethernet communication hardware.