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 healthcare diagnostics has confirmed low frequency of barcode read errors with the dimension vista tobr flex reagent cartridge lot 13095ab and dimension vista crbm flex reagent cartridge lot 13095ac. if the impacted flex reagent cartridge cannot be read the instrument will post a "bad barcode" error on the instrument screen. the impacted flex reagent cartridge will not be loaded on the dimension vista.