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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.
The most serious of the three kinds is the Class I remember.
Avanos Medical pulled Cortrak* 2 EAS out of service due to the deaths of patients and injuries related to nasogastric tube misplacements.
The device was designed to aid trained health care workers in placing medical feed tubes for patients.
However, the wrong placement of nasogastric or nasoenteric tubes could cause damage to the vocal cords of a patient and trachea or lungs, resulting in serious injury or even death.
The company has recall 629 devices, which were sold in the US from April 1st, 2016 until 1 January 2022.
Avanos Medical The company recall communication stated that 60 patients were injured and 23 of them died as a result of incorrect placement in nasogastric tube while using Cortrak* 2 EAS.
Avanos Medical will revise the labelling after the recall. Avanos Medical feeding tube This will include updating the instructions on use and intended use of Cortrak* 2 EAS.
https://www.rheingoldlaw.com/blog/2022/may/avanos-faces-fda-class-i-recall-after-23-deaths-/ The updated guidelines require users to verify the location of tubes in accordance with protocols of their institutions before making use of them.
Cortrak 2 eternal access system Avanos Medical has its headquarters in Alpharetta Georgia. Avanos Medical sells its products across more than 90 countries.
The company reached an agreement with OrthogenRx to purchase the company in a $160m transaction. Avanos Medical closed the acquisition on January 20th.
My Website: https://avanos.com/investor-news/response-to-inquiries-about-the-avanos-cortrak-2-voluntary-field-correction/
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