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Avanos Medical and FDA issued a Class 1 recall of 629 units of CORTRAK*2 an enteral access device, which is a feeding tube positioning device that is linked to many injuries and deaths.
https://www.pcb.its.dot.gov/PageRedirect.aspx?redirectedurl=https://www.nsmedicaldevices.com/news/avanos-medical-cortrak-2-eas-class-i-recall/ These devices were distributed between April 1, 2016, until January 1, 2022. They're used to assist healthcare professionals place feeding tubes into the stomach or intestines of patients.
Incorrect placement of nasogastric and nasoenteric tube has been responsible for more than 60 injuries and 23 deaths in the last year.
Cortrak 2 eternal access system Avanos Medical feeding tube placement This recall will be used to change the information on the device so that it reminds users to ensure that the tube was properly placed before they can deliver nutrients.
https://peatix.com/user/15855343 According to FDA the adverse events were respiratory failure and pneumothorax (collapsed lungs), perforation [a hole in the wall or bowel of the lung], pneumonia (a lung infection), and the pleural effusion (excess fluid in the space between your lungs and your chest cavity).
Avanos Medical feeding tube 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].
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