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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Complaints were received for the same batch of v40 lfit vitallium femoral heads (part number 6260-9-032 lot 48681201) alleging that the femoral head could not be assembled with its corresponding v40 stem trunnion.