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 i (b7399) of panocell-20 lot 35385 is listed as jka negative on the master list. post-release testing of the cell has identified that this donor possesses a weak expression of the jka antigen and the cell does not react with some examples of anti-jka.