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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2 customer complaints in total were received from distributors located in germany and rance with regard to inconsistent results from the expected results on the destiny plus analyzer whilst running a prothrombin time (pt assay). these incidences were noted on the mechanical mode of the instrument.