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Avanos is in danger of FDA Class I recall after 23 deaths related to the device
The Avanos Medical Cortrak*2 Ental Access System was created to assist trained health professionals with the placement of medical feeding tubes in patients' small intestines or stomachs. Avanos Medical feeding tube There were 23 deaths attributed to feeding tubes since 2015.

There have been numerous reports of injury and death among patients who had their nasogastric tubes misplaced.

This recall is used to modify the labels of the device, such as the directions for use and the intended use. Avanos Medical Avanos Medical Users are instructed to verify that the tube is placed in accordance with the guidelines of their establishment prior to applying it to provide nutrition.

Avanos Medical Patients may suffer serious injuries or even death if a nasogastric tube or nasoenteric tub has been incorrectly installed.

https://www.ormanager.com/briefs/fda-updates-safety-alert-for-cortrak-2-enteral-access-system/ The recall notice from Avanos Medical said that there were sixty-three injuries and 23 deaths linked to the misplacement or removal of the nasogastric feed tube during usage of the CORTRAK*2 Entral Access System. This occurred since the year 2015. Pneumothorax (collapsed lung) also known as pneumothorax ("collapsed lung") perforation ("hole in the wall, or the bowels of the lung), pneumonia (a bacterial infection in the lungs) and pleural fluid (excess fluid between the lungs).

Avanos Medical feeding tube Avanos Medical, on March 21st, 2022, issued a corrective field notification to its customers who used these products between January 2021 and January 2022. The notice included the following information:

Place nasogastric or nasoenteric tubs in accordance with the institution's policies.
Cortrak 2 eternal access system Avanos Medical feeding tube Attach the corrective notice in the field in the operator's manual.
Avanos Med will ask you to return the acknowledgment sheet that was sent with your email notification.
Website: https://www.fdanews.com/articles/207866-avanos-medical-gets-class-i-designation-for-its-recalled-cortrak2-enteral-access-system?v=preview
     
 
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