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Avanos Medical and the FDA have issued a Class 1 recall for approximately 629 units of the CORTRAK*2 Entral Access System, a feeding tube placement device that is associated with dozens of accidents and deaths.
Avanos Medical Avanos Medical The recalled devices were distributed between April 1st, 2016 and January 1, 2022. These devices can be used by healthcare professionals to insert feeding tubes inside the stomach or intestines.
Avanos Mediacal Cortrak 2 Since the year 2015, there have been 20 deaths and 60 injuries recorded due to nasogastric and nasoenteric tubes that were not placed correctly.
Avanos Medical feeding tube This recall is used to update the information on the device to remind users to verify that the tube was properly placed before they can deliver the food.
Avanos Medical According to FDA, "Adverse events include pneumothorax, respiratory failure perforation (a hole or puncture within the lung's wall, esophagus or the bowel) or pneumonia, lung infection, and pleural effusion ("excess fluid between the 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 [email protected].
Read More: https://static.foxnews.com/foxnews.com/content/uploads/2022/04/Avanos_CORTRAK2_Field_Correction_Letter.pdf
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