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Avanos Medical and the FDA have issued a Class 1 recall for about 629 units of the CORTRAK*2 Entral Access System, a feeding tube placement device responsible for dozens of fatalities and injuries.
Cortrak 2 eternal access system The devices were released between April 1, 2016 between January 1st, 2022 and April 1, 2016. Avanos Mediacal Cortrak 2 feeding tube placement They're used to aid healthcare professionals place feeding tubes in the stomach or intestines of patients.
https://static.foxnews.com/foxnews.com/content/uploads/2022/04/Avanos_CORTRAK2_Field_Correction_Letter.pdf Since the year 2015, there have been 23 deaths and 60 injuries reported in cases where nasogastric tubes or nasoenteric were placed incorrectly.
The recall is used to alter the device's label , which instructs users to confirm that the tube was properly placed prior to delivering food.
According to FDA, adverse events included respiratory failure as well as pneumothorax (collapsed lung tissue) Perforation (a hole in the bowel or wall of the lungand pneumonia (a lung infection) and the pleural effusion (excess liquid that has accumulated in the lung space and your chest cavity).
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].
My Website: https://static.foxnews.com/foxnews.com/content/uploads/2022/04/Avanos_CORTRAK2_Field_Correction_Letter.pdf
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