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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Synthes is initiating a voluntary recall of the flexible grip (part number 355.28) which is part of the universal nail system. synthes received notification from its supplier that this recall is due to the potential lack of clean-ability of the class i reusable manual surgical instrument.