Avanos Medical, FDA and Avanos Medical, FDA and the FDA have issued a Class 1 Recall for approximately 629 units CORTRAK*2 Ental Access System. Avanos Medical feeding tube This feeding tube positioning device has been linked to multiple deaths and injuries. Avanos Medical feeding tube The devices for recall were distributed between April 1 2016, through January 1, 2022. https://washingtonindependent.com/deadliest-fda-recalls-2022-misplaced-feeding-tubes-leading/ They are used to help healthcare professionals insert feeding tubes into the stomach or the intestines in patients. Avanos Medical Nasogastric or Nasoenteric tubes that were placed incorrectly have resulted in 23 deaths and 60 injury reports since 2015. The recall is being used to change the label on the device to inform users to verify that the tube is properly placed prior to delivering food. Avanos Medical feeding tube According to FDA adverse events, they include respiratory failure as well as pneumothorax (collapsed lungs) Perforation (a hole in the wall or bowel of the lung], pneumonia (a lung infection), and Pleural effusion (excess fluid in the space between your 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 gpms-ha-reporting@avanos.com. Cortrak 2 eternal access system
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