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 have been rare occurrences where a microslide cartridge is misidentified after entering microslide cartridge lot information in the "manually load cart" dialogue. when this issue occurs it is possible for the vitros 5600 integrated system (software version 1.5 and below) and vitros 51 fs chemistry system (software version 2.5 and below) to process results from a cartridge other than the intended cartridge potentially leading to erroneous patient results.