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Avanos Medical, FDA and the FDA have issued an Class 1 Recall for 629 units of CORTRAK*2's Ental Access System. Avanos Medical feeding tube feeding tube placement Avanos Medical This feeding tube placement device has been linked to many deaths and injuries.
The recall devices were released beginning on April 1 in 2016 until January 1, 2022. Avanos Mediacal Cortrak 2 These devices can be used by health professionals to insert feeding tubes inside the stomach or intestines.
https://www.nsmedicaldevices.com/news/avanos-medical-cortrak-2-eas-class-i-recall/ Incorrect placement of nasogastric as well as Nasoenteric tubes has been responsible for more than 60 injuries and 23 deaths since 2015.
This recall is used to correct the information on the device in order to remind users to ensure that the tube has been set before they can provide the food.
https://www.fda.gov/medical-devices/medical-device-recalls/avanos-medical-recalls-cortrak2-enteral-access-system-risk-misplaced-enteral-tubes-could-cause Avanos Medical According to FDA, "Adverse events include pneumothorax, respiratory failure perforation (a hole or puncture in the lung wall, esophagus, or bowel) and pneumonia, lung infection and the pleural effusion ("excess fluid that is accumulating between the lungs and 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].
My Website: https://medicaldevices.icij.org/devices/hkg-cortrak-2-enteral-access-system-eas
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