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 identified a need to provide specific instructions for initiating power to the calcar planer prior to engagement with bone in the cutting edge omnifit hfx secur-fit max/secur-fit plus max and omnifit eon surgical protocols as well as to provide specific instructions for rasping dense bone and/or narrow intramedullary canals for the accolade surgical protocol.