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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원인
Incorrect product labelling. the outer corrugate box label is correct however the inner unit package label references an incorrect product code. the inner unit package identifies product code 54-5036r but should be 54-3650r.