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 is conducting a field correction for the advia centaur homocysteine (hcy) assay for the 1:10 dilution recovery used on the advia centaur advia centaur xp and advia centaur cp systems. siemens has confirmed that the percent recovery for the 1:10 diluted patient sample dilutions is lower than reported in the instructions for use.