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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Bd has confirmed through complaint investigation that during the manufacturing process portions of the test slides in the above referenced products were placed into the incorrect product packaging. this could result in intermittent quality control failures and false results.