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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A product correction notice has been issued because of a problem with microslide reagent management on the vitros 5600 integrated system (software version 1.3.2 and below) and on the vitros 51 fs chemistry system (software version 2.5 and below). under certain condition the affected systems may process results from a cartridge other than the intended cartridge.