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Avanos Medical, FDA and the FDA have issued a Class 1 Recall for 629 units CORTRAK*2 Ental Access System. This feeding tube positioning device has been linked to many deaths and injuries.
The recall devices were made available from April 1 2016, through January 1, 2022. Avanos Medical These devices are utilized by health professionals to insert feeding tubes into patients' stomachs or in the intestines.
Since 2015, there have been 20 deaths and 60 injuries recorded for nasogastric or nasal tubes that were placed incorrectly.
Cortrak 2 eternal access system Avanos Medical The recall will change the label on the device so that it can instruct users to verify that the tube is correctly placed before delivering nutrition.
Avanos Medical According to FDA adverse events, they include respiratory failure and pneumothorax (collapsed lung tissue), perforation [a hole in the wall or bowel of the lungas well as pneumonia (a lung infection) and the pleural effusion (excess fluid in the lung space and your 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
Homepage: https://www.medtechdive.com/news/avanos-medical-recall-class-i/623892/
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