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 received a small number of complaints about calibration failure with n latex b2 microglobulin. in rare cases the signal generated at the highest calibration point can exceed the analog-digital converter capacity of an affected bn system. this effect does not allow the establishment of a calibration curve due an invalid calibration point measurement.