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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Carefusion has identified an issue with the alaris syringe pump module 8110 software versions 9.15 and 10.5. infusion can unexpectedly stop when an infusion is transitioning from one state to another.