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 is conducting a recall for advia 1800 and advia 2400 ise firmware v2.23. advia chemistry chloride electrodes may fail prematurely during calibration due to a chloride bias parameter error. the operator will receive an ng flag which requires immediate action to be taken on the calibration samples.