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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In isolated incidences (less than 0.003%) while using the device in nmba monitoring mode electrodes used may deterioate to a level where current densities may be large enough to cause superficial burns on the skin of the patient.