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Avanos Medical Recalls Cortrak*2 Enteral Access Systems
According to the U.S. Food & Drug Administration (FDA), Avanos Medical is recalling the Cortrak*2 Enteral Access System because the misplacement of nasogastric or nasoente tubes has led to accidents and deaths of patients. Cortrak 2 eternal access system The recall includes 629 devices that were available in the United States.

Avanos has marketed the Cortrak*2 Enteral Access System, which is known for its screen-based visualization of the stomach or small bowel, which can aid in the proper placement of a medical feeding tube. feeding tube placement Patients may experience injuries to their vocal chords or trachea if the tube was installed improperly. Avanos Medical released a recall statement stating that there had been sixty incidents and 23 deaths caused by misplacement, in 2015, because of the CORTRAK*2 Entry Access System. Cortrak 2 eternal access system Pulmonary failure, pneumothorax (collapsed lungs) and perforation (a hole in the esophagus or bowel wall) pneumonia, an excess of fluid in the lung and chest cavity (the chest cavity and the lung tissue) have all been among the injuries.

Avanos Medical feeding tube feeding tube placement Avanos Medical has described a plan to provide users with updated labeling, to confirm the correct placement of nasogastric and nasoenteric tubes before use

The Avanos warning is the second warning that the FDA issued in 2022 about the use of enteral feeding tubes. The FDA advised healthcare professionals and parents of the risk of strangulation among children who are fed through tubes. https://zephyrnet.com/sv/fda-identifies-avanos-medicals-cortrak-2-eas-recall-as-class-i/ Two cases of strangulation in children occurred in 2021. They were as a result of a tube system that wrapped around a patient's neck.

FDA Recalls Avanos Medical Device

Ental Feeding Delivery Sets

Cortrak* 2 Enteral Access System Product Details

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