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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Teleflex medical is issuing an advisory notification to customers who have received the affected products because of an awareness of a minimal discrepancy between the labeled cuff diameter and the actual cuff diameter of the endotracheal tube.