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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The product labeled as 4024-908 lot#2002afk contains the incorrect bracket model. the packaging is labeled as 4024-908 for the lower right 1st bicuspid (lr4) -12t/2a but incorrectly contains part 4024-910 for the lower right 2nd bicuspid (lr5) -17t/2a.