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's smartsite needlefree connector component 2000e found in these kits are under recall. the smartsite connector may unintentionally disconect from a female luer during infusion. an inability to disconnect may require replacement of a line.