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Avanos Medical has recalled the Cortrak*2 Ental Access System in response to the risk of injuries and deaths resulting from the misplacement of the nasoenteric as well as na tube. The recall currently comprises 629 devices distributed across the United States.
Avanos Mediacal Cortrak 2 Avanos has marketed the Cortrak*2 Entraal Access System that assists with the installation of a medical-feeding tube. Patients could suffer damage to their vocal chords, lungs or the trachea if the tube is not correctly placed. Avanos Medical released a recall statement stating that there had been a total of 60 accidents and 23 deaths resulting from mistaken placement, in 2015, due to the CORTRAK*2 Entry Access System. Cortrak 2 eternal access system There have been several incidents, including respiratory failure, pneumothorax or collapsed lung, perforation (a hole in the lungs' wall or the bowel) pneumonia, and the pleural effusion. Avanos Medical This is an excess of fluid between your lungs as well as the chest cavity.
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 caution the FDA issued in 2022 concerning the use of enteral feeding tubes. The FDA sent out a message to healthcare professionals and parents regarding the danger of strangulation in the event that feeding tubes are being used by children. Cortrak 2 eternal access system Two cases of child strangulation was reported in 2021. It was caused by a tubing system that was wrapped around the neck of a patient.
feeding tube placement FDA Recalls Avanos Medical Device
The potential risk of Enteral Feeding Delivery Sets
Cortrak* 2 Enteral Access System Product Details
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Read More: https://www.justice.gov/opa/pr/avanos-medical-inc-pay-22-million-resolve-criminal-charge-related-fraudulent-misbranding-its
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