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 has confirmed that the dimension vista flex hcys reagent cartridge catalog # k7044 lot number 15243ma shows a reduced open well stability that does not meet the claimed time frame. as a consequence qc recoveries can be found below the assigned ranges giving invalid runs that may prompt customers to a new calibration.