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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Since the exipration date of the buterfly needle is not the same as the prosthesis and the external retail box label has the expiry date of the prosthesis only the kits is mislabelled with the expiration date that matches the implant and not the butterfly needle.