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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Under specific rare conditions which require a system reset there is a potential for a sample to be dispensed into an aliquot well that has previously been used for a qc or calibrator product from a dimension vista vial. if two samples are dispensed into the same aliquot well the first sample will always be qc or calibrator from a dimension vista vial. patient sample will never be dispensed into an aliquot well that contains another patient sample. the issue is in vista sw 3.5.1 and sw 3.6.