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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Some issues have been reported when firmware version 3.13 was installed on systems equipped with the old transient recorder (tr) board (ref. 6200350). extenisve testing has proven that firmware 3.13 may potentially cause an instrument to freeze or hang during acquisition when installed with the old tr board with a risk repeated results for different spots.
Model Catalog: 410710 (Lot serial: S/N BELOW 50039 AND ABOVE); Model Catalog: 410895 (Lot serial: 60000 ARE CONCERNED); Model Catalog: 410710 (Lot serial: 60000 ARE CONCERNED); Model Catalog: 410895 (Lot serial: EXCEPTION 50050 IS ALSO); Model Catalog: 410710 (Lot serial: EXCEPTION 50050 IS ALSO); Model Catalog: 410895 (Lot serial: CONCERNED.); Model Catalog: 410710 (Lot serial: CONCERNED.); Model Catalog: 410895 (Lot serial: S/N BELOW 50039 AND ABOVE)