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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Due to customer complaints reporting that the double swivel connector may crack or separate on the endobronchial tube. should this occur the device may leak causing a risk of respiratory distress or hypoxia that can in some cases lead to the need to re-intubate the patient.