Notes

Avanos Medical Recalls Cortrak*2 Enteral Access Systems
Avanos Medical is recalling Cortrak*2 Entry Access System. The FDA declares that patients have suffered injuries and killed due to nasogastric or the nasoenteric tube being misplaced. The recall currently includes 629 devices which were sold in the United States.

Avanos marketing its Cortrak*2 Endural Access System has been primarily for the on-screen images of stomachs of patients and small bowels, which aid in the placement of medical feeding tubes. Cortrak 2 eternal access system Patients are at risk of damage to their vocal chords, lungs, or the trachea, if a tube is not properly placed. Avanos Medical recalls that there are 60 incidents, 23 deaths and 23 illnesses that were caused by the misplacement or inadvertent insertion of a feeding tube for nasogastric patients using the CORTRAK*2 Enteral Access System. The injuries include respiratory failure, pneumothorax and perforation. Avanos Medical feeding tube All of these are forms of lung collapse.

Avanos Medical outlined a plan which would permit patients to have updated labeling so they are able to confirm the position of nasogastric, nasoenteric and other tubes before they are used

Avanos is the second warning issued by the FDA has issued in relation to feeding tubes that are intra-oral. In February the FDA issued a warning for parents and healthcare providers regarding the possibility of strangulation in the event that children are fed through feeding tubes. Two cases of strangulation by a child were reported in 2021. The reason for this was a tubing system that was wrapped around the neck of the patient.

FDA Recalls Avanos Medical Device

Potential risk of enteral Feeding Delivery Sets

Cortrak* 2 Enteral Access System Product Details

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