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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Ge healthcare has recently become aware of a potential safety issue wherein the oxygen and air wall or tank inlet fittings on the back panel were reversed during assembly. as a result this may potentially have reversed air/oxygen gas concentrations for example a setting of 100% oxygen could have an output of 21% oxygen and vice versa. the settings of the blender knob will no longer be accurate.