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 has confirmed that for multifibren u (catalog numbers owzg19 owzg23) fibrinogen calibrator kit (catalog number oqvk11) and control plasma n (catalog numbers orke41 orke45) users may receive a number of error messages when measuring a calibration curve on the behring coagulation system (bcs) and bcs xp instruments.