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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Blister package of 439 catalog numbers and lots of burs may not be completely sealed thereby potentially compromising the sterility of the devices. recalled burs have exp. dates between may 2008 and nov 2010.