Notes

Avanos is in danger of FDA Class I recalls following 23 deaths related to the device
Avanos Medical Cortrak*2 enteral access system is designed to allow health professionals to place medical feeding tubes into the small intestine or stomach of patients who require nutritional assistance. Avanos Medical feeding tube Since 2015, however 23 patients have died due to complications related to feeding tube.

Numerous reports have indicated that patients have suffered trauma or even died when their nasogastric or nasoenteric tubes were misplaced. This is despite the fact the device was designed to aid in their placement.

This recall is used to change the device's labels, including the instructions for usage and the intended usage. Avanos Medical https://www.fda.gov/medical-devices/medical-device-recalls/avanos-medical-recalls-cortrak2-enteral-access-system-risk-misplaced-enteral-tubes-could-cause The updates instruct users to confirm tube placement according to the protocols of their institution prior to using the tube to deliver nutrition.

Avanos Mediacal Cortrak 2 Incorrectly inserting a Nasogastric or Nasoenteric tube could result in damage to the vocal chords, lungs or trachea. https://arcieve.blogspot.com/2022/05/avanos-medical-recalls-cortrak2-enteral.html This could lead to grave injury and possibly death.

Avanos Medical has issued a recall notice stating that as of 2015, there have been sixty deaths and 23 injuries resulting from an incorrect placement of the nasogastric feeding tube. Avanos Medical Affected events include respiratory failure and pneumothorax (collapsed lung) and perforation (a hole in the lung's wall or esophagus) and pneumonia (a lung infection), and the pleural effusion (excess fluid that has accumulated in the lung space and the chest cavity).

Avanos Medical sent a field correction notice on the 21st of March 2022 to customers who had utilized the devices between January 2021 and January 2022. https://www.newsbreak.com/news/2607393691988/avanos-medical-recall-of-cortrak-2-enteral-access-system-is-class-i These instructions were included in the notification:

Verify the placement of nasogastric/nasoenteric in accordance with institutional policies
Attach the corrective notice in the field of the operator's handbook.
Avanos Med will require you to return the acknowledgement sheet included with the email notice.
My Website: https://goalz.online/avanos-medical-faces-class-i-recall-for-feeding-tube-system-linked-to-23-deaths-since-2015-fiercebiotech/