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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Ortho-clinical diagnostics has identified two scenarios on the vitros 5600 integrated system (software version 1.4 and below) and vitros 3600 immunodiagnostic system (software version 1.4 and below) in which microwell and/or microtip reagent inventory may not be properly updated resulting in misidentified reagent packs and incorrect results or 'no result' being reported by the system.