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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Manufacturer has received reports of the thread length protruding past the dome of the acetabular trial or implant. it was determined that the press fit between the threaded stud and the handle shaft assembly for the trident universal impactor/positioner (p/n: 2101-0200) may lead to the gradual protrusion of the threaded stud over time.