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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A false reaction maybe observed with the mica019 antigen. upon investigation trnsfected mica 019 cell lines (rc1223) demonstrated a lack of or presence of recombinant mica019 inserts.