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Avanos Medical and FDA issued a Class 1 recall of 629 units CORTRAK*2 enteral access system, which is a tube for feeding device that has been implicated in numerous accidents and deaths.
The devices were made available between April 1, 2016, until January 1, 2022. feeding tube placement Avanos Mediacal Cortrak 2 https://www.pcb.its.dot.gov/PageRedirect.aspx?redirectedurl=https://www.medicaldevice-network.com/news/fda-avanos-medical-cortrak2-eas-recall/ These devices are used by health professionals to insert feeding tubes into the stomachs of patients or their intestines.
Since 2015, there have been 20 deaths and 60 injuries reported due to nasogastric and nasoenteric tubes that were improperly placed.
The recall is being used to change the label of the device, which will instruct users to verify that the tube is properly set up prior to feeding.
https://www.inventables.com/users/figueroacarter9275 According to FDA, "Adverse events include respiratory failure, pneumothorax perforation (a perforation or hole that is located in the lung wall, esophagus, or the bowel) or pneumonia, lung infection, and the 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]. feeding tube placement feeding tube placement
Read More: https://www.inventables.com/users/figueroacarter9275
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