Notes

Avanos is in danger of FDA Class I recall following 23 deaths linked to the device
The Avanos Medical Cortrak*2 Ental Access System was designed to aid trained health care professionals in placing medically-approved feeding tubes in patients' small intestines or stomachs. Since 2015, however 23 people have died from complications related to feeding tube.

There have been numerous reports of injuries to patients and deaths following misplacement or misalignment of nasogastric, also known as the nasoenteric tubes. Avanos Medical Avanos Mediacal Cortrak 2 They are utilized to assist in the placement of their tubes.

Cortrak 2 eternal access system This recall is being utilized to create updates to the device's labeling, which includes the directions for use and intended uses. It is recommended that users verify that the tube is placed according to the protocols of their institute prior to applying it to provide nutrition.

If you do not insert correctly a Nasogastric tube or Nasoenteric tube may cause harm to the vocal chords, lungs , or the trachea. This could result in severe injury or even death.

Avanos Mediacal Cortrak 2 Avanos Medical's recall notice stated that there were more than 23 deaths and 60 injuries caused by the misplacement, or removal of the nasogastric feed tubes in the usage of the CORTRAK*2 Entral Access System. Avanos Medical This occurred in 2015. There were a variety of adverse events that occurred, including respiratory failure, pneumothorax (collapsed lungs) and perforation (a hole or opening in the esophagus's wall or bowel) or pneumonia, as well as pleural effusion (excess liquid in the air space between your lungs and chest cavity).

https://www.nsmedicaldevices.com/news/avanos-medical-cortrak-2-eas-class-i-recall/ On March 21 2022 Avanos Medical issued a field correction notification to its customers who had used the devices between January 2021 and January 2022. The notice contained the following guidelines:

Verify the location of Nasogastric tubes and the nasoenteric tube according to institution policies.
Avanos Medical feeding tube Include the field correction notice concerning the problem to the operator's manual.
Avanos Med will require that you return the acknowledgment sheet included with your emailed notice.
Here's my website: https://www.fdanews.com/articles/207866-avanos-medical-gets-class-i-designation-for-its-recalled-cortrak2-enteral-access-system?v=preview