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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Cell 5 (donor b3907) of lot 29304 is demonstrating weak positive reactions in direct antiglobulin testing (dat). tests performed with this cell may produce unexpected positive reactions at the ani-human globulin (ahg) phase of testing.