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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There is a potential issue with an aesthetic dot at the back of the blade. potential for this dot to become loose or fall out after autoclave. this could occur on about 10% of all manufactured blades. may pose potential risk if not monitored.