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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There are mixed syringe barrel/tip types in this product: barrels with oral syringe tip and barrels with luer slip tip (i.E. during manufacture bulk luer slip tip syringe components were inadvertently mixed in with bulk oral syringe components prior to barrel printing). both are printed "for oral use only".