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FDA has identified Avanos Medical’s Cortrak*2 EAS recall Class I

Avanos Medical recalls Cortrak*2 EAS in the wake of reports of injury and even death caused by tube misplacements.

The US Food and Drug Administration (FDA) has identified the recall of Avanos Medical's Cortrak* 2 Enteral Access System (EAS) as a Class I recall.

A Class I can remember is considered to be to be the most important of all three classes.

feeding tube placement Cortrak 2 eternal access system Avanos Medical recalls Cortrak*2 EAS after reports of injury and deaths due to incorrect placements of nasogastric or nasal tubes.

The device was developed to aid trained health professionals in putting medical feed tubes into patients.

However, incorrectly installed nasogastric/nasoenteric pipe could result in damage to the vocal cords and trachea. https://www.inventables.com/users/dotsonfitzpatrick6398 This can lead to serious injuries or even death.

Avanos Medical feeding tube The company is recalling 629 devices, which were made available in the US from April 1st, 2016 until 1 January 2022.

In the recall announcement the company said that since 2015 there have been 60 injuries as well as 23 deaths due to the improper placement or use of nasogastric feeding tube while using the Cortrak* 2 EAS.

In the wake of the recall, Avanos Medical will update the device's labelling. This will include updating instructions regarding the use and intended uses of the Cortrak*2 EAS.

The updated guidelines also instruct users to confirm tube placement based on the respective institution's protocols before usage.

Avanos Mediacal Cortrak 2 Avanos Medical has its headquarters in Alpharetta Georgia. Avanos Medical's well-known brands are accessible in over 90 countries.

The company agreed to buy OrthogenRx for $160 million in December. feeding tube placement Avanos Medical closed the acquisition on January 20th.


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