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Avanos Medical has recalled the Cortrak*2 Ental Access System due to accidents and deaths that result from misplacement of nasoenteric and nasogastric tube. The recall covers 629 devices which were distributed in the United States.
Avanos marketing its Cortrak*2 Endural Access System has been for its on-screen visualizations of patients' stomachs and small bowels, which aid in the placement of medical feeding tubes. If the tube is not placed correctly, it can cause damage to vocal cords, lungs and the trachea. Avanos Medical has reported that there have already been 60 injuries and 23 deaths caused by misplacement of feeding tubes for nasogastric patients using CORTRAK*2's Ental Access System. The injuries can be described as respiratory failure, pneumothorax and perforation. Cortrak 2 eternal access system Cortrak 2 eternal access system These are all forms of lung collapse.
Avanos Medical feeding tube Avanos Medical feeding tube Avanos Medical outlined a plan that will allow patients to get updated labels so they can confirm the placement of nasogastric, nasoenteric , and other tubes prior to when they are employed
Avanos is the FDA's second warning regarding insertal feeding tubes. In February, parents as well as healthcare professionals were warned by the FDA about the possibility of strangulation of children who use tubes for feeding. Two deaths of children from strangulation were reported in 2021. as a result of a tube system that wrapped around a patient's neck.
Avanos Medical feeding tube FDA Recalls Avanos Medical Device
Enteral Feeding Delivery Sets
Cortrak* 2 Enteral Access System Product Details
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Read More: https://www.fda.gov/medical-devices/medical-device-recalls/avanos-medical-recalls-cortrak2-enteral-access-system-risk-misplaced-enteral-tubes-could-cause
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