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 is informing customers that identified product code / lot number combinations of magic3 intermittent catheters may have a sterile barrier breach where the catheter may be caught in the seal or protruding from the seal of the packaging and potentially have the catheter tip cut.