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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Specific product code / lot number combinations of bard dualok breast lesion localization wires may be at risk of having portions of the wire protruding from the packaging thus representing a breach of the sterile barrier and potential sharps hazard.