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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Following an internal investigation the elecsys t3 assay (cat # 07027869190) will need to have a correction of the unit of measure for the cross-reactant rt3 value included in the methodsheet of the cobas e810 module(corrected from ug/dl to ug/ml).