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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Teleflex is conducting a voluntary recall for certain lots of teleflex sutures because they did not meet minimum needle attachement strength requirements. if affected product is used the needle may become detached from the suture during use.