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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Genesee biomedical has issued an advisory concerning use of the sternal valve retractor with atrial and aortic attachments because corrosion was found to have caused failure in a retractor blade. hospitals should not use blades that are corroded or damaged.