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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For the lot 28105900 the reagent buffer bottles has been mislabeled. the r1 bottle is labeled as r2/ed instead of r1/ed and the r2 is labeled r1/ea instead of r2/ea.