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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In the software screens on cobas e 602 the expiry date of ft4 ii reagent kit lot 188609 could be displayed 11/2016 instead of the correct date 10/2016 which is the expiry date of the box and the reagetn kit label. when this occurs the false expiry date is used with the reagetn kits.