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 control vlaues prot1 con h may be found out of range ( >+/- 15%) for dimension vista prealb flex reagent cartridge leading to invalid runs. we have no indication that other analytes in prot1 con h are affected by this issue.