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 manufacturer has received one complaint that the trocar tip had fallen off during a surgical procedure. as a consequence the tip needed to be removed in an additional surgical procedure. the trocar tip was detached from the trocar shaft due to a fracture in the weld seam between the tip and shaft.