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Avanos Medical and the FDA have issued a Class 1 recall for 629 units of the CORTRAK*2 Entral Access System, a feeding tube placement device responsible for dozens of fatalities and injuries.
Avanos Medical feeding tube Avanos Medical These devices were introduced between April 1, 2016, to January 1, 2022. Avanos Mediacal Cortrak 2 They're used to aid healthcare professionals to insert feeding tubes into the stomach or intestines of patients.
https://www.indiegogo.com/individuals/31107010/ Avanos Mediacal Cortrak 2 The incorrect placement of the nasogastric tube and Nasoenteric tubes has been the source of more than 60 injuries and 23 deaths since 2015.
https://app.glosbe.com/profile/7005043825353690333 The recall is being used to change the device's label , which instructs users to make sure that the tube has been placed correctly before delivering nutrition.
https://independent.academia.edu/CoyleIbsen According to FDA, adverse events included respiratory failure, pneumothorax (collapsed lung) perforation (a hole in the bowel or wall of the lung], pneumonia (a lung infection) and the pleural effusion (excess liquid that has accumulated in the space between your 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]. https://www.inventables.com/users/laustengreen2153 https://www.ted.com/profile
Homepage: https://bbs.pku.edu.cn/v2/jump-to.php?url=https://www.click4r.com/posts/g/7258766/avanos-recalls-cortrak-2-over-potential-enteral-tube-misplacement
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