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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Bard has identified that the product code/lot number combination listed may have the wrong size catheter inside. there have been reports where the product indicates a catheter size of 14fr but a smaller size catheter of 12fr was packaged instead. product return is not required.