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FDA classifies Avanos Medical's cortrak*2 EAS recall as Class 1.

Avanos Medical called off Cortrak* 2 EAS in response to the patient injury and deaths caused by tube malfunctions.

Cortrak 2 eternal access system The US Food and Drug Administration has identified the Cortrak*2 of Avanos Medical's enteral access system (EAS), for recall as a Class II recall.

Avanos Mediacal Cortrak 2 A Class I remember is considered to be to be the most important of the three classes.

Avanos Medical recalls Cortrak*2 EAS after reports of injury and death due to incorrect placements of nasogastric or nasal tubes.

The device allows healthcare personnel to place medical feeding tubes inside patients.

Cortrak 2 eternal access system Avanos Mediacal Cortrak 2 However, improper placement of nasogastric and nasoenteric tubes can damage the vocal cords of patients or trachea, lungs, or vocal cords and cause severe injuries or even death.

Avanos Medical feeding tube In total, the company has recalls 629 devices sold in the US between April 1st, 2016 and 1 January 2022.

The company also said in a recall notice that there had been more than 23 patients and 60 injuries who died since 2015 due to the incorrect placement of nasogastric feed tubes in the Cortrak* 2 EAS.

Avanos Medical, following the recall, will be updating the device’s labelling. Avanos Medical feeding tube This includes an update of the instructions and the planned applications of Cortrak* 2 EAS.

The revised guidelines also direct users to verify the placement of their tubes according to the institution's protocols before usage.

Cortrak 2 eternal access system Avanos Medical has its headquarters in Alpharetta Georgia. Avanos Medical markets its well-known brands in more than 90 countries.

Cortrak 2 eternal access system Cortrak 2 eternal access system The company agreed to buy OrthogenRx for $160 million in December. Avanos Medical successfully closed the acquisition of OrthogenRx in January.


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