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Avanos Recalls FDA Class II Following 23 Deaths Associated with the Device

 The Avanos Medical Cortrak*2 Ental Access System was designed to assist trained health care professionals in placing medically-approved feeding tubes in the small intestines of patients or stomachs. There have been 23 deaths reported to date due to feeding tubes in 2015. There have been many incidents of death and injuries in patients who have lost their nasogastric tube. This recall is used for updates to the device's labeling, which includes the instructions for use. Avanos Medical feeding tube Users are instructed to verify that the tube is set according to the protocols of their establishment prior to applying it to provide nutrition. Avanos Medical Avanos Medical The patient's vocal cords, lungs and trachea could be damaged when the nasogastric/nasoenteric tube is installed improperly. Avanos Medical Avanos Medical This can result in serious injury or even death. Avanos Medical feeding tube Avanos Medical feeding tube Avanos Medical's recall communication said that there were sixty injuries, 23 deaths, and 58 patients who were injured due to the incorrect placement of the nasogastric tubes. The CORTRAK*2 enteral access system has been in operation since 2015. Pneumothorax (collapsed lung) also known as pneumothorax (collapsed lung), perforation (hole in the wall or the bowels of the lung) as well as pneumonia (a bacterial infection in the lung) and the pleural fluid (excess fluid in between the lungs). Avanos Medical feeding tube Avanos Medical issued on March 21, 2022, a field correction notice to its customers who were using the devices between January 20,21 and January 20,22. The following instructions were contained in the notice: Verify the placement of nasogastric/nasoenteric in accordance with institutional policies Attach the pertinent field correction notice to the operator's guide. Please return the acknowledgement page along with the email notice to Avanos Medical

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