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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The master list packaged with panocell-10 (lot 13083) contains a typographical error in the antigen typing listed for cell 5 (donor e791). the donor e791 typing is incorrectly listed as positive for the f antigen. the antifen status for donor e791 should be listed as f negative.