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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Stryker howmedica osteonics has become aware that there was a cross mix between the osteonics series 7000 total knee standard tibial tray and the triathlon total knee system primary cemented tibial base-plate. the packaging was labeled as a series 7000 total knee standard tibial tray while the package actually contained a triathlon total knee system primary cemented tibial base-plate.