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Avanos Medical has recalled the Cortrak*2 Ental Access System because of injuries and deaths caused by misplacement of nasoenteric and nasogastric tube. The recall covers 629 devices, which were distributed throughout the United States.
feeding tube placement Avanos marketing its Cortrak*2 Endural Access System has been primarily for its on-screen visualizations of patients' stomachs and small bowels, to assist in the placement medical feeding tubes. Avanos Medical feeding tube If the tube is not placed correctly, it can result in damage to vocal cords, lungs , and the trachea. Cortrak 2 eternal access system Avanos Medical's recall notification states that since 2015, there have been 60 patient deaths and 23 injuries due to the incorrect placement of nasogastric feed tube when using the CORTRAK*2 access system. The causes of the injuries are pneumothorax, respiratory failure and perforation. These are all types of lung collapse.
Avanos Medical describes a plan to revise labeling in order to make sure that the tubes for nasogastric and nasoenteric before the use
The Avanos warning was the second FDA warning in 2022 regarding feeding tubes for the enteral system. feeding tube placement In February, the FDA issued a warning to healthcare professionals and parents about the risk of strangulation in children who use feeding tubes. Two instances of strangulation in children that involved feeding tubes wrapped around the necks of patients have been reported by 2021.
FDA Recalls Avanos Medical Device
The potential risks of entering Sets of Feeding Delivery
Cortrak* 2 Enteral Access System Product Details
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