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Avanos Medical Recalls Cortrak*2 Ental Access System
Avanos Medical (U.S. Food & Drug Administration) has announced that it is recalling Cortrak*2's Enteral Access System. The recall was announced because of injuries to patients and death from misplaced nasoenteric/nasogastric tubes. Cortrak 2 eternal access system The recall covers 629 devices sold in the United States.

Avanos Mediacal Cortrak 2 Avanos sells its Cortrak*2 enteral access device for its visualization of the small bowel as well as stomach, which aids in the placement of a feeding tube. Patients could suffer damage to their vocal cords, lungs, or the trachea if the tube is not correctly placed. Avanos Medical recalls that there are 60 accidents, 23 deaths, and 23 illnesses related to the improper placement or accidental inserting of a feeding tube for nasogastric patients using the CORTRAK*2 Entral Access System. There have been a variety of injuries, including pneumothorax, respiratory failure, collapsed lung perforation (a opening in the wall of your lungs or bowel), pneumonia and the pleural effusion. This is an excess of fluid between your lungs and the chest cavity.

Avanos Mediacal Cortrak 2 Avanos Medical outlined a plan that would allow users to get updated labels so they are able to confirm the position of nasogastric, nasoenteric , and other tubes before they are used

Avanos is the second alert that the FDA has issued in relation to intra-oral feeding tubes. In February, parents and healthcare professionals were advised by the FDA about the potential for strangulation of children using tubes for feeding. Two cases were reported of strangulation among children who had a feeding tube wrapped around their necks.

FDA Recalls Avanos Medical Device

The Risks of Enteral Feeding Delivery Sets

Cortrak* 2 Enteral Access System Product Details

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