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Avanos Medical called off Cortrak* 2 EAS as a result of patient injury and deaths caused by tube misplacements.
Avanos Mediacal Cortrak 2 The US Food and Drug Administration (FDA), has declared the recall of Avanos Medical of Cortrak*2 Ental Access System, (EAS), as an class I recall.
A Class I can remember is considered to be the most serious of all three classes.
Avanos Medical recalled Cortrak* 2 EAS after incidents of injury and patient deaths due to nasoenteric or nasogastric tube misplacements.
https://www.kickstarter.com/profile/830556256/about The device was designed to assist health care professionals when placing medical feed tubes for patients.
However, incorrectly installed nasogastric/nasoenteric pipe could result in damage to the vocal cords, or trachea. https://classifieds.lt/index.php?page=user&action=pub_profile&id=4281498 Avanos Mediacal Cortrak 2 This can lead to grave injuries or even death.
The company recalls 629 devicesthat were made available across the US between 1 April 2016 to 1 January 2022.
The recall communication from the company also stated that there were sixty injuries and 23 deaths of patients since the year 2015 due to misplacement of the nasogastric feeding tubes when using the Cortrak* 2 EAS.
Avanos Medical will revise the labelling following the recall. This includes changing the instructions for Cortrak*2 EAS as well as its intended uses.
Users are also directed to ensure that the tubes are installed in accordance with the protocols of the institution before they utilize them.
Headquartered in Alpharetta, Georgia, US, Avanos Medical focuses on the production of medical devices that are clinically proven. feeding tube placement Avanos Medical sells its products across more than 90 countries.
The company agreed to buy OrthogenRx for $160 million in December. Avanos Medical closed on the acquisition in January.
https://dohabb.com/index.php?page=user&action=pub_profile&id=1036421
Website: https://classifieds.lt/index.php?page=user&action=pub_profile&id=4281498
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