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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Intuitive surgical is initiating a voluntary correction regarding the use of certain da vinci endowrist instruments with a cardiac cryoablation probe. intuitive surgical has determined that microscopic metallic particulate can be generated during both robotic and non-robotic intra-cardiac surgery. the use of da vinci instruments other than the cardiac probe grasper (e.G. large needle driver) to manipulate a cardiac cryoablation probe during da vinci cardiac surgery has been shown to increase the amount of microscopic metallic particulate.