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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It was determined that fine plastic strands inside the endotracheal tube side of the airway adapter may become dislodged and subsequently inhaled by the patient. the strands are typically 5mm long and 100 microns in diameter about the thickness of a human hair.