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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D711 reference membranes may cause the status value of the ph electrolyte electrodes to be offset resulting in calibration failure. root cause was an error in the formulation of the inner solution.