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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Cadence science inc. was notified by a customer that the graduation marks of the syringe are not centered with the numeric position marks on the syringe barrel. while the graduation marks are correctly space for volume the numeric marks do not correctly align. this could cause the user to either under or over dose.