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 healtcare diagnostics received a customer complaint regarding versacell and the advia chemistry 1800 system. if the versacell is connected to an advia 1800 chemistry analyzer an incorrect sample tube may be pipetted.