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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There is analytical sensitivity greater than 0.50 ng/ml described in the instructions for use when the affected calibrator c lots are used with advia centaur ferritin on the advia centaur cp system only. this does not apply to the advia centaur or advia centaur xp systems.