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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Interlink system micro-infusion manifolds that are connected together in series may loosen or disconnect at the luer connection if the manifolds are twisted in an attempt to align the interlink ports after the luer connectors have been tightened. loosening or disconnection may result in a leak.