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Avanos Medical has recalled Cortrak*2 EAS due to reports of deaths and injuries caused by tube displacements.
Cortrak 2 eternal access system The US Food and Drug Administration has classified Avanos Medical’s Cortrak*2 Enteral Access System (EAS), as a Class 1 recall.
A Class I remember is the most serious type out of the three classes.
Avanos Medical called off Cortrak* 2, EAS after deaths and injuries that resulted from the misplacement of tubs for nasogastric surgery.
The device is able to assist trained health care professionals in placing medical feeding tubes into patients. It also gives real-time information about tube placement.
However, the incorrect placement of the nasogastric or nasoenteric tubes could cause severe injury or death.
Cortrak 2 eternal access system The company has recalled 629 devices distributed throughout the US between January 2016 and January 2022.
The communication regarding the recall from the company added that there had been 60 injuries and 23 deaths of patients since the year 2015 due to the misplacement or misplacement the nasogastric feeding tubes when using the Cortrak* 2 EAS.
Avanos Medical will revise the labelling in the wake of the recall. Cortrak 2 eternal access system This will include updating Cortrak*2 EAS's instructions and expected uses.
Users are also advised to ensure that the tubes are installed in accordance with the protocols of the institution prior to use.
Cortrak 2 eternal access system The headquarters are located in Alpharetta, Georgia, US, Avanos Medical focuses on manufacturing clinical medical devices. Avanos Medical Its brands are available across more than 90 countries.
Avanos Medical feeding tube The company signed an agreement to purchase OrthogenRx at $160 million during December. Avanos Medical closed the acquisition on the 20th of January.
https://aacnjournals.org/ajcconline/article/29/1/22/30624/Pneumothoraces-Prevented-With-Use-of
Website: https://www.medtechdive.com/news/avanos-medical-recall-class-i/623892/
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