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Avanos Medical called off Cortrak* 2 EAS in response to patient deaths and injuries 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 an I Class recall.
A Class 1 recall is the most serious of the three classes.
Avanos Medical called off Cortrak* 2, EAS following injuries and deaths resulting from the misplacement of nasogastric tubs.
The device was designed to assist healthcare professionals with training to insert medical tube feedings inside patients. It also provides live information about the tube's location in real-time. placement.
Avanos Mediacal Cortrak 2 The wrong placement of Nasogastric tube and nasoenteric tube could cause serious injury , or even death.
https://list.ly/goldenfink348 The company has now recalled 629 devices from the US which were distributed between 1 April 2016 - 1 January 2022.
http://ezproxy.cityu.edu.hk/login?url=https://www.medicalbuyer.co.in/fda-identifies-avanos-medicals-cortrak-2-eas-recall-as-class-i/ According to the recall notice the company has stated that in the year 2015, there have been 60 injuries and 23 deaths as a result of the improper placement or use of nasogastric feeding tube while making use of the Cortrak* 2 EAS.
Avanos Medical will revise the labelling in the wake of the recall. feeding tube placement This includes updating the instructions on use and intended use of Cortrak* 2 EAS.
The new guidelines direct users to confirm that the tube was placed according to the protocols of their institution prior usage.
Avanos Medical has its headquarters in Alpharetta Georgia. The company has more than 90 markets to sell its renowned brands.
The company signed an agreement with OrthogenRx to acquire the company for $160 million in a deal. https://www.ted.com/profile Avanos Medical closed on the acquisition in January.
https://www.indiegogo.com/individuals/30833058/
Read More: https://www.inventables.com/users/hovgaardmcwilliams1458
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