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 that dimension vista chem 1 cal lots 5gm081 and 5gm082 may produce depressed results with current lots of calium reagent. although the affected chem 1 cal lots are expired the calium calibration internval is 90 days therefore it is possible that calibrations using the calibrator lots are active.