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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Smith & nephew became aware of new information relating to the performance of birmingham hip modular head (bhmh). recent registry and clinical data showed a decline in the performance of the bhmh. based on its analysis of this information smith & nephew considers that patients implanted with the bhmh device may be at greater risk of revision surgery.