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Avanos Medical and FDA issued a Class 1 recall of 629 units of CORTRAK*2 the enteral access system. Avanos Mediacal Cortrak 2 It is a tube for feeding device that has been linked to numerous injuries and deaths.
https://list.ly/dowlingmejia370 The recall devices were released from April 1, 2016 to January 1, 2022. Avanos Medical Cortrak 2 eternal access system https://lexsrv3.nlm.nih.gov/fdse/search/search.pl?match=0&realm=all&terms=https://washingtonindependent.com/deadliest-fda-recalls-2022-misplaced-feeding-tubes-leading/ These devices can be utilized by healthcare professionals to place feeding tubes into the stomach or intestines.
Nasogastric tubes, also known as Nasoenteric tubes, that were not properly placed have led to the deaths of 23 people and 60 injury incidents since 2015.
Avanos Medical feeding tube This recall is used to change the label on the device in order to remind users to ensure that the tube was properly placed before they can deliver nutrition.
According to FDA, adverse events included respiratory failure and pneumothorax (collapsed lung tissue) and perforation, a hole in the bowel or wall of the lung], pneumonia (a lung infection) and Pleural effusion (excess fluid in the lung space and the 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]. Avanos Mediacal Cortrak 2
Read More: https://list.ly/dowlingmejia370
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