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Avanos Medical is recalling Cortrak*2 Entry Access System. The FDA declares that patients have suffered injuries and killed due to nasogastric or an nasoenteric tube that was misplaced. The recall covers 629 devices that were sold in the United States.
Avanos marketing the Cortrak*2 Endural Access System has been for the on-screen images of stomachs of patients and small bowels to aid in the placement of medical feeding tubes. However, patients could suffer from damage to their vocal cords and lung if the tube is not properly placed. Avanos Medical recalls that there are 60 incidents, 23 deaths and 23 illnesses that were caused by the improper placement or accidental inserting of a nasogastric feeding tube using the CORTRAK*2 Entral Access System. https://www.misterpoll.com/users/avanos medical feeding tubetqsf6776 The injuries have included respiratory failure and pneumothorax (collapsed lung), perforation (a hole in the lung's wall, esophagus or the bowel) as well as pneumonia. an effusion of the pleura (excess fluid in the chest cavity and the lungs).
Avanos Medical described a plan for users to receive updated labeling to confirm proper use of the nasogastric tube and nasoenteric tubes prior to use.
http://hawkee.com/profile/1851946/ Avanos is the second alert that the FDA has issued in relation to intra-oral feeding tubes. http://pandora.nla.gov.au/external.html?link=https://24x7mag.com/standards/fda-updates/avanos-medicals-enteral-access-system-gets-fda-class-i-recall/ The FDA sent out a message to parents and healthcare providers regarding the danger of strangulation in the event that feeding tubes are being used by children. Two cases of strangulation in children were reported in 2021. https://bbs.pku.edu.cn/v2/jump-to.php?url=https://www.medscape.com/viewarticle/891200 This was due to tubes that were placed around the neck of a patient.
FDA Recalls Avanos Medical Device
Risk of entering feed delivery sets
Cortrak* 2 Enteral Access System Product Details
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Homepage: http://hawkee.com/profile/1851946/
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