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 orthopedics has become aware that there is the potential for the presence of a burr in the last threaded feature of restoration modular cone body trials. this threaded feature mates with the trial locking bolt. to date no product experience reports have been received with regard to this issue.