Notes

Avanos Medical recalls the Cortrak*2 entry access system
Avanos Medical (U.S. Avanos Medical Avanos Mediacal Cortrak 2 Food & Drug Administration) has announced that it is recalling Cortrak*2's Enteral access system. This recall was initiated in response to injuries sustained by patients and death from misplaced nasoenteric/nasogastric tubes. Avanos Medical feeding tube https://www.newsbreak.com/news/2607393691988/avanos-medical-recall-of-cortrak-2-enteral-access-system-is-class-i Avanos Mediacal Cortrak 2 The recall covers 629 devices distributed in the United States.

Avanos has launched the Cortrak*2 Entraal Access System that assists with the placement of a medical feeding tube. https://www.justice.gov/usao-ndtx/pr/avanos-medical-pay-22-million-resolve-criminal-charge-related-fraudulent-misbranding Patients may however be harmed to their vocal cords as well as lungs if the tube is not properly inserted. Avanos Medical recalls that there are 60 injuries, 23 deaths and 23 illnesses resulting from the improper placement or accidental inserting of nasogastric feeding tube while using the CORTRAK*2 Entral Access System. Pneumothorax (collapsed lung) or pneumothorax, perforation (a gap or hole within the wall of a lung), pneumonia, and the pleural effusion (excess liquid in the lungs, chest cavity) are some of the incidents.

Avanos Mediacal Cortrak 2 Avanos Medical has presented a plan to offer users updated labeling to ensure the proper placement of nasogastric (and the nasoenteric) tubes prior to using them.

Avanos Mediacal Cortrak 2 Avanos is the FDA's second caution about insertal feeding tubes. The FDA cautioned parents and healthcare professionals about the risk of strangulation for children who are fed through tubes. Two deaths of children from strangulation were reported in 2021. as a result of a tube device that was wrapped around the patient's neck.

FDA Recalls Avanos Medical Device

Potential Risk of Enteral Feeding Delivery Sets

Cortrak* 2 Enteral Access System Product Details

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