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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To notify customers of an additional statement in the warning/precautions section of product labeling for multi-length ureteral stents. end users should consider the presence of a knot if significant resistance is encountered during attempts at removal. product return is not requested as part of this notification.