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 complaint was received indicating that the box labelled with part number 825-0625 which is the red band #25 tip gutta percha but actually contains blue-band #30 tip gutta percha part number 825-0630.