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Avanos fails to meet FDA Class 1 Recall Resulting in 23 deaths attributed to the Device
Avanos Medical Cortrak 2 Entry Access Systems is designed to aid trained health professionals in inserting medical feed tubes in the small bowel or stomach of patients who are requiring nutrition. There were 23 deaths attributed to the feeding tube in the year 2015.

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

Avanos Medical feeding tube This recall is being used for updates to the labeling of the device, which includes the instructions on how to use it. Cortrak 2 eternal access system The new instructions advise users to verify the tube's placement according to the protocols of their institution prior to using the tube to provide nutrition.

Patient's vocal cords, lungs, and the trachea can be damaged if the nasogastric/nasoenteric tube was placed improperly. Avanos Medical feeding tube Avanos Medical Avanos Medical This could result in grave injury or even death.

Avanos Medical has issued a recall communication stating that since 2015, there has been 60 patient deaths and 23 injuries resulting from the wrong placement of the nasogastric tube. Respiratory failure, pneumothorax perforation (a hole, or hole in the stomach wall) and pneumonia were all reported.

Avanos Medical issued on March 21, 2022, a correction notice to its customers using these devices between January 20,21 and January 20,22. Avanos Medical feeding tube The notice provided the following information:

Place nasogastric or nasoenteric tubs according to the policies of the institution.
Cortrak 2 eternal access system Attach the relevant field correction notice to the operator’s guide.
Avanos will need to acknowledge receipt of the email notice.
My Website: https://www.yourlawyer.com/lawsuits/avanos-medical-recalls-the-cortrak2-enteral-access-system/
     
 
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