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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It has been identified that the shaft tip material (casting) does not meet the smith & nephew endoscopy division 416 material specification and therefore results in the rusting of the distal end of the tendon stripper.