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 renew product number 3262 (long fenestrated grasper) was packaged and labelled as product number 3642 (super-atrau fenestrated grasper). the renew product number 3642 (super-atraumatic fenestrated grasper) was packaged and labelled as 3262 (long fenestrated grasper).