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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Siemens healthcare diagnostics received customer complaints regarding dimension clinical chemistry system total iron binding capacity (ibct) flex reagent cartridges (df84). siemens has confirmed an increased incidence in "abnormal reaction" test report messages on some heparinised plasma samples as compared to the matched serum samples.