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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Discrepancy between some of the flow sets in valves manufactured between january 2009 and october 2010. this flow rate deviation may cause patients to receive a smaller or larger dose of medicinal oxygen.