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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Separation of the iv cannula from the needle hub when the button is pressed inability of the needle to puncture the skin as it slides back into the hub and partial activation of the devices in packaging. in several instances the needle remained in the arm of the patient.