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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The third party supplier for material used to manufacture the restoration modular components has demonstrated poor process control which has raised concerns about the quality of the raw material supplied. as a precaution and due to the potential impact on the mechanical properties of the affected products stryker is recalling all products manufactured from material supplied by this supplier.