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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 that were sold in the United States.
Avanos Medical feeding tube Avanos selling its Cortrak*2 Endural Access System has been primarily for the on-screen images of stomachs and small bowels to aid in the placement of medical feed tubes. Cortrak 2 eternal access system Avanos Mediacal Cortrak 2 Avanos Mediacal Cortrak 2 If the tube is not placed correctly, it can result in damage to vocal cords, lungs , and the trachea. Avanos Medical released a recall announcement stating that there have been sixty incidents and 23 deaths caused by the misplacement of a tube in 2015 due to the CORTRAK*2 Access System. The injuries have included respiratory failure and pneumothorax (collapsed lung), perforation (a hole in the wall of the lung, esophagus, or bowel) as well as pneumonia. pleural effusion (excess fluid in the chest cavity and the lungs).
Avanos Medical feeding tube Avanos Medical describes a plan to revise labeling in order to ensure proper placement of nasogastric or nasoenteric tube before it is used.
feeding tube placement Avanos is the FDA's second caution about inserting feeding tubes. In February, the FDA issued a warning to parents and healthcare professionals regarding the risk of strangulation when children are fed by feeding tubes. feeding tube placement Two child strangulation deaths occurred in 2021. They were due to a tubing device that was wrapped around the patient's neck.
FDA Recalls Avanos Medical Device
The potential risk of Enteral Feeding Delivery Sets
Cortrak* 2 Enteral Access System Product Details
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