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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Mini mix kits were inadvertently labeled with the term "assorted kit" rather than the correct shade designation a2. however although the sytringes themselves are missing the a2 shade designation the outer package for the kits correctly indicates the correct shade of the product inside.