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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Precipitates have been identified in affected vials consisting of fibrin. samples containing precipitates allow for an increased frequency of functional disturbances (error messages e.G. clot error etc.) to be expected in the instruments.