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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Two reported incidences in which the sideplate did not mate properly with the corresponding hip screw. the discrepancy was in the barrel of the sideplate which was manufactured slightly undersized.