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Avanos Medical and the FDA have issued a Class 1 recall of 629 units of the CORTRAK*2 Enteral Access System, a feeding tube placement device responsible for dozens of deaths and injuries.
Cortrak 2 eternal access system https://www.medtechdive.com/news/avanos-medical-recall-class-i/623892/ Avanos Mediacal Cortrak 2 The recall devices were distributed on April 1st from 2016 to January 1, 2022. https://www.mpo-mag.com/contents/view_breaking-news/2022-05-16/avanos-recalls-cortrak2-over-potential-enteral-tube-misplacement/ Avanos Medical They're used to assist medical professionals insert feeding tubes in the stomach or the intestines of patients.
Avanos Medical Nasogastric tubes, also known as Nasoenteric tubes, that were improperly placed on the market have led to 20 deaths and 60 injury incidents since 2015.
The recall is being used to alter the device's label , which instructs users to ensure that the tube was properly set up prior to feeding.
https://www.weitzlux.com/firm-news/cortrak2-enteral-access-system/ Avanos Medical According to FDA the adverse events include respiratory failure as well as pneumothorax (collapsed lungs) perforation (a hole in the wall or bowel of the lungor bowel of the lung (a lung infection) and Pleural effusion (excess fluid in the lung space 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://www.dmagazine.com/healthcare-business/2021/07/medical-device-company-to-pay-22-million-for-mislabeling-gowns/
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