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 older version of the device has a design defect which allows for a fatigue related failure. there are two screws that attach the cage to the bracket which may fatigue over time and fail causing the cage to become detached from the mount and fall.