Notes

Avanos fails to meet FDA Class 1 Recall Due to 23 Deaths Associated with the device
Avanos Medical Cortrak 2 Entry Access Systems is created to assist trained healthcare professionals to insert medical feeding tubes into the small bowel or stomach of patients who require nutrition. Cortrak 2 eternal access system In 2015, there have been 23 deaths related to the feeding tube.

Many reports have revealed that patients suffered injuries or even passed away after their nasogastric or nasoenteric tubes were misplaced. Avanos Medical feeding tube It's despite the fact this device was utilized to aid in their placement.

This recall is utilized to create updates to the device's labeling, which includes the instructions for use and intended uses. Cortrak 2 eternal access system The updated instructions instruct users to confirm tube placement in accordance with the guidelines of their institution prior to using the tube for delivering nutrition.

If a nasogastric tube is placed incorrectly it is possible for patients to suffer injury to the vocal cords, lungs, or trachea, all which can lead to serious injury or death.

The recall notice from Avanos Medical declared that there were sixty-three injuries and 23 deaths due to the misplacement or removal of the nasogastric feed tube during use of the CORTRAK*2 Enteral Access System. Avanos Medical https://www.yourlawyer.com/lawsuits/avanos-medical-recalls-the-cortrak2-enteral-access-system/ This occurred in the year 2015. The adverse events that were reported include respiratory failure pneumothorax (collapsed lung) and perforation (a hole in the wall of the lung, esophagus, or bowel), pneumonia (a lung infection), and pleural effusion (excess fluid that has accumulated in the space between the lungs and the chest cavity).

Avanos Medical, on March 21, 2022, sent a field correct notification to its customers who used these products between January 2021-January 2022. Avanos Medical feeding tube The following information was included in the notification.

https://www.medicaldevice-network.com/news/fda-avanos-medical-cortrak2-eas-recall/ Confirm placement of the nasogastric, nasal and other tubes in accordance with institutional guidelines.
Attach the corrective notice within the field of the operator's handbook.
Avanos Medical Return the acknowledgement form included with the notice emailed to Avanos Medical
Website: https://www.yourlawyer.com/lawsuits/avanos-medical-recalls-the-cortrak2-enteral-access-system/