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 has initiated a voluntary product field correction for the xia titanium 4.5 vitalium rod 4.5 x 600 mm. the pre-cut / straight xia 4.5 rods were changed as a part of a marketing request so that they would be dimensionally and visually consistent to the new pre-cut / pre-bent xia 4.5 rods released as a part of a separate change.