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 potential risks with model code 2420-0500 for multiple lot numbers. breakages and cracks in the spin luer may lead to the administration set disconnection and/or leakage of infusate. the disconnection and leakage may be observed during infusion.