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.
데이터 추가 비고
원인
Synthes (canada) ltd. received notification from its supplier synthes gmbh that a medical device recall was being initiated for the transpedicular schanz screw dual core due to complaints received that the fracture clamp could not be used with the screw. in some cases the shaft of the screw is too thick.