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 fabius gs or fabius tiro delivered between june 2005 and june 2006 could have been equipped with a power cord of the manufacturer electri-cord manufacturing corporation (ecm). the us food and drug administration (fda) has associated a risk of sparks fire device failures or electrical shocks with these power cords. although drager medical has not received any reports of failures of power cords manufactured by ecm drager medical will replace the possible affected power cords.