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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Updating the instructions for use for the pressure display box and disposible sets included in the sorin group usa custom perfusion tubing pack for the revolution centrfugal blood pump. the update will reflect the current performance of the display box.