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 helathcare diagnostics has confirmed the possibility of variability in recovery of qc and patient results with the dimension vista csa flex reagent cartridge lots 12300bb 12318bb and 13011bb. internal studies have shown an upward trend in recovery over the three day open well set claim.