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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The devices being recalled are surgical clip appliers that are preloaded for use in minimally invasive surgical procedures. teleflex is recalling these devices because they have a nonconformity that may cause clips to misload jam or fall out of the appliers.