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 received customer feedback on the advia centaur systems c-peptide assay indicating a low but increased rate of signal 2 errors. a limited number of customers have experienced the signal 2 error codes. patient results cannot be generated if a signal 2 error is obtained. this issue has not been observed on the advia centaur cp.