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 specific product code / lot number combinations of magic3 hydrophilic-coated female intermittent catheters that may be at risk of having a small void in the package seal and thus product sterility may be affected.