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Avanos Medical is recalling Cortrak*2 Entry Access System. The FDA says that patients have been injured and killed by nasogastric or nasoenteric tube misplacement. The recall covers 629 devices sold in the United States.
Avanos Medical feeding tube Avanos is promoting the Cortrak*2 Ental Access System because of its ability to see the stomach and small bowel. This allows for the placement of an medical feed tube. Patients could suffer damage to their vocal cords, lungs, or trachea if a tube is not properly placed. Avanos Medical has reported that there have already been sixty-three injuries and 23 deaths caused by misplacement of feeding tubes for nasogastric patients using the CORTRAK*2 Ental Access System. Cortrak 2 eternal access system These injuries include respiratory failure, pneumothorax (collapsed lung), perforation (a hole in the wall of the lung, esophagus or the bowel) as well as pneumonia. the pleural effusion (excess fluid between the chest cavity and the lungs).
Avanos Medical feeding tube Avanos Medical has described a plan to offer users current labeling to verify the correct placement of nasogastric and nasoenteric tubes prior to use.
The Avanos warning was the second FDA warning in 2022 concerning enteral feed tubes. The FDA warned parents and healthcare professionals about the risk of strangulation among children who feed tubes. Avanos Medical Two deaths resulting from strangulation of children was reported in 2021 as a result of the tube being placed 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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Website: https://www.supplychain.nhs.uk/icn/avanos-medical-uk-ltd-factory-closure-on-entral-branded-products/
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