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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Performed investigations have shown that the two hip elements may have a negative effect on the venous backflow under certain conditions. therefore it cannot be excluded that the shape of the hip elements may be considered as a contributing factor to thromboembolic events.