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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Certain lots of teleflex sutures did not meet minimum diameter requirements. if affected product is used and failure occurs delay in procedure wound dehiscence bleeding and/or infection may occur requiring medical and/or surgical intervention.