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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One lot of scalpel packages labeled as ck-3 large full radius scalpel part # 975-0011 actually contained ck-6 small full radius scalpel. the package listed the correct part number but included the incorrect part.