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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Internal testing has shown that when running an average of more than 70 samples per day a bias of sodium of more than 2mmol/l may occur.
Model Catalog: S7770 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: 962-169 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: S5362 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: S4970 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: S1730 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: S1720 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: RADIANCE (Lot serial: ALL SERIAL NUMBERS); Model Catalog: 962-170 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: 393-825 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: 393-726 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: 393-725 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: 393-721 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: 393-720 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: 393-706 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: 393-705 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: 393-701 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: 393-700 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: S7370 (Lot serial: ALL SERIAL NUMBERS)