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 received customer complaints for lfit v40 vitallium femoral heads (manufactured july 7th 2014 - august 15th 2014). it was reported that the femoral head could not be assembled with its corresponding v40 stem trunnion at the time of surgery. in each case a new v40 lfit vitallium femoral head was opened and used.