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Avanos Medical is recalling Cortrak*2 Entry Access System. The FDA says that patients have suffered injuries and even killed by nasogastric and the nasoenteric tube being misplaced. The recall includes 629 devices sold in the United States.
Avanos selling the Cortrak*2 Endural Access System is known for the on-screen images of patients' stomachs and small bowels, which assist in the placement medical feeding tubes. Avanos Medical Patients may experience harm to their vocal cords or trachea if the tube was installed incorrectly. Avanos Medical recalls that there are sixty accidents, 23 deaths, and 23 illnesses related to the improper placement or accidental inserting of nasogastric feeding tube while using the CORTRAK*2 Entral Access System. https://www.medicaldevice-network.com/news/fda-avanos-medical-cortrak2-eas-recall/ Injuries have included respiratory failure pneumothorax (collapsed lung) and perforation (a hole in the lung's wall, esophagus, or bowel) as well as pneumonia and an effusion of the pleura (excess fluid between the chest cavity and the lungs).
Avanos Medical feeding tube Avanos Medical described a plan for users to get updated labeling to confirm proper placement of the nasogastric tubes and nasoenteric tubes prior to use.
Avanos is the FDA's second warning regarding insertal feeding tubes. Avanos Medical In February, the FDA issued a cautionary note to parents and healthcare professionals about the risk of strangulation when children are fed through feeding tubes. Two instances of strangulation by children involving feeding tubes wrapped around the necks of patients have been reported before 2021.
FDA Recalls Avanos Medical Device
Potential risk of enteral feeding delivery sets
Cortrak* 2 Enteral Access System Product Details
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Here's my website: https://www.ecri.org/search-results/member-preview/hrcalerts/pages/hrcalerts011718_fda
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