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Avanos faces FDA Class I recalls following 23 deaths related to the device
The Avanos Medical Cortrak*2 Ental Access System was designed to assist trained health professionals with the placement of medical feeding tubes into patients' small intestines or stomachs. Since 2015, however 23 people have passed away due to complications related to feeding tube.

Avanos Mediacal Cortrak 2 Avanos Mediacal Cortrak 2 Numerous reports have indicated that patients have sustained trauma or even died when their nasogastric or nasoenteric tubes were not properly placed. Avanos Medical It's despite the fact that this device was used to aid in the placement.

https://americanews.news/avanos-medical-recalls-cortrak-2-enteral-access-system-for-risk-of-misplaced-enteral-tubes-could-cau-14041.html This recall is used to make changes to the device's labels, including the directions for use and the intended usage. The new instructions advise users to check the placement of the tube based on their institution's protocols before using the tube to deliver nutrition.

Avanos Medical feeding tube If a nasogastric, or nasoenteric tube is not inserted correctly the patient could suffer damage to vocal cords, lungs, or trachea, all which can lead to serious injuries or even death.

According to the Avanos Medical recall notice There were 60 injuries and 23 patient deaths related to the incorrect placement of nasogastric feed tubes while making use of the CORTRAK* 2 Enteral Access System, since 2015. There have been several adverse events that occurred, including respiratory failure, pneumothorax (collapsed lung tissues), perforation (a gap or opening in the esophagus's wall or the bowel), pneumonia, and the pleural effusion (excess fluid in the space between your lungs and the chest cavity).

Avanos Medical feeding tube Avanos Medical, on March 21st, 2022, issued a field correct notice to customers who had used the products between January 2021-January 2022. The notice provided the following guidelines:

Check the positioning of nasogastric and nasoenteric tubes according to institutional guidelines.
Add the notice of correction for field regarding the issue to the operator's guide.
Avanos will need to acknowledge receipt of the email message.
My Website: https://biotech-insider.com/avanos-medical-faces-class-i-recall-for-feeding-tube-system-linked-to-23-deaths-since-2015/                      
     
 
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