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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This recall/product correction is related to a new drug interference that was identified for indocynanine green (icg) in all direct and total bilirubin tests performed on roche platforms (cobas c cobas integra and modular p systems).