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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The reflex hybrid screw extractor inner shaft was reported to fail at the threaded tip and fracture in the head of the screw. there had been reports of the threaded tip of the inner shaft being left in the screw due to the surgeon being unable to remove the screw. there had also benn reports of damage to the screw and/or the plate while attempting to remove the screw.