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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If pump is used with extracorporeal membrane oxygenation it is possible for ecmo circuit to generate enough negative pressure to pull syringe plunger from holder resulting in uncontrolled fluid flow.