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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Certain lot numbers of the individual syringe packages labelled to contain the illumina 150ml linden luer syringe with handi-fil straw catalogue number 900103 may contained the similar product the illumena 150ml regular luer syringe with handi-fil straw catalogue number 900101.