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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Labelling correction was being initiated due to the product label referencing the incorrect raw material of 316l-astm f138. the raw material should be co-20cr-15w-10ni-astm f90.