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Avanos MedicalAfter 23 deaths, Feeding Tube Placement Devices are Recalled
Avanos Medical, FDA and the FDA have issued an Class 1 Recall for approximately 629 units CORTRAK*2 Ental Access System. Avanos Medical https://www.fda.gov/medical-devices/medical-device-recalls/avanos-medical-recalls-cortrak2-enteral-access-system-risk-misplaced-enteral-tubes-could-cause This feeding tube-placement device has been linked to many deaths and injuries.

Avanos Medical The recalled devices were distributed between April 1st 2016, 2016 until January 1, 2022. The devices are utilized by healthcare professionals to insert feeding tubes into stomachs or intestines.

Avanos Medical feeding tube Nasogastric tubes or Nasoenteric tubes that were improperly placed on the market have led to the deaths of 23 people and 60 injury incidents since 2015.

This recall will be used to change the information on the device, in order to remind users to ensure that the tube is correctly put in place before they could deliver nutrients.

https://www.techtimes.com/articles/275216/20220509/cortrak-2-eas-from-avanos-medical-raises-patient-safety-concerns.htm According to FDA, "Adverse events include pneumothorax, respiratory failure, perforation (a perforation or hole that is located in the lung wall, esophagus or the bowel), pneumonia, lung infections, and the pleural effusion ("excess fluid between the lungs, and the chest cavity),"

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 feeding tube
Read More: https://www.fdanews.com/articles/207866-avanos-medical-gets-class-i-designation-for-its-recalled-cortrak2-enteral-access-system
     
 
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