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 outer diameter (od) documented on the tray inner and outer box labels did not match the od printed on the tube flange. the od stated on the labelling is 11.0mm and the od of the tube is actually 11.8mm.