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Avanos MedicalRecall of Feeding Tube Devices After 23 Fatal Accidents
Avanos Medical, FDA and Avanos Medical, FDA and the FDA have issued an Class 1 Recall for about 629 units of the CORTRAK*2 Ental Access System. Cortrak 2 eternal access system This feeding tube-placement device has been linked to numerous injuries and deaths.

The devices that were recalled were released between April 1 in 2016 and January 1, 2022. https://www.techtimes.com/articles/275216/20220509/cortrak-2-eas-from-avanos-medical-raises-patient-safety-concerns.htm Avanos Medical feeding tube Cortrak 2 eternal access system The devices are used by healthcare professionals to insert feeding tubes inside the stomach or the intestines.

Avanos Medical feeding tube The incorrect placement of the nasogastric tube and Nasoenteric tubes has been the source of 53 deaths and 60 injuries since the year 2015.

Avanos Medical feeding tube The recall is used to update the label of the device to inform users to ensure that the tube is correctly placed prior to feeding.

https://www.fdanews.com/articles/207866-avanos-medical-gets-class-i-designation-for-its-recalled-cortrak2-enteral-access-system "Adverse events that were reported included respiratory failure and pneumothorax (collapsed lung) perforation (a hole in the wall of the lung or esophagus or bowel) as well as pneumonia (a lung infection) and an effusion of the pleura (excess fluid that is leaking from the lung cavity and chest cavity)," according to the FDA.

For more information, customers with questions or concerns about this recall should contact Avanos Medical by phone at 470-448-5444 or by emailing [email protected]. Avanos Medical
Website: https://www.fda.gov/medical-devices/medical-device-recalls/avanos-medical-recalls-cortrak2-enteral-access-system-risk-misplaced-enteral-tubes-could-cause
     
 
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