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Avanos Medical and FDA issued a Class 1 recall of 629 units CORTRAK*2 an enteral access device, which is a feeding tube placement device that has been linked to numerous accidents and deaths.
Avanos Medical feeding tube The devices were released between April 1, 2016, to January 1, 2022. https://www.yourlawyer.com/lawsuits/avanos-medical-recalls-the-cortrak2-enteral-access-system/ Avanos Medical feeding tube These devices can be utilized by healthcare professionals to insert feeding tubes in the stomach or the intestines.
Cortrak 2 eternal access system Avanos Medical Incorrect placement of nasogastric and Nasoenteric tube was the source of more than 60 injuries and 23 deaths since the year 2015.
The recall will change the label on the device to remind users to check that the tube has been correctly placed prior the time of delivering nutrition.
"Adverse events reported included respiratory failure as well as pneumothorax (collapsed lung), perforation (a hole in the wall of the lung, esophagus, or bowel) as well as pneumonia (a lung infection) and pleural effusion (excess fluid that is leaking from the lung cavity and chest cavity)," according to the FDA.
Cortrak 2 eternal access system 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].
Read More: https://aacnjournals.org/ajcconline/article/26/2/149/3230/Cortrak-Assisted-Feeding-Tube-Insertion-A
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