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 reports of breakages of the distal end of the avs tl spacer trial during the trialing step of the procedure. during insertion or removal of the trial into the disc space the joint between the handle and paddle can break at the weld.