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 extension set tubing that connects to the t adapter is not completely inserted into the receptive area of the t adapter. the tubing disconnects from this jonction results in leakage blood or solution.