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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There is a typographical error on the supplemental unconfirmed typings for cell 9 (donor b1356). the donor is listed as rg+ and should be listed as rg-. the accompanying master list correctly lists cell 9 as rg- in the special type column.