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Avanos Medical pulled Cortrak*2 EAS off service following reports about injuries and deaths caused by tube displacements.
The US Food and Drug Administration has acknowledged the Cortrak*2 of Avanos Medical's Enal Access System Recall (EAS) as Class I recall.
The most severe of the three types is the Class I remember.
Avanos Medical pulled Cortrak* 2 EAS from service after patient deaths and injuries due to nasogastric tubes misplacements.
https://odolbodol.shop/index.php?page=user&action=pub_profile&id=2111506 The device is intended to aid healthcare professionals with training to insert medical tubes for feeding inside patients. It also provides the most current information about tube placement.
However, the incorrect placement of the nasogastric, or nasoenteric tube could result in severe injuries or even death.
Avanos Mediacal Cortrak 2 The company has now removed 629 devices from the US which were distributed between April 1st, 2016 and 1 January 2022.
According to the recall communication the company has stated that as of 2015, there had been 60 injuries and 23 deaths resulting from the incorrect placement or misuse of the Nasogastric feeding tubes while using the Cortrak* 2 EAS.
In the wake of the recall, Avanos Medical will update the device's labelling. Avanos Mediacal Cortrak 2 This includes changing the instructions as well as the intended uses for Cortrak* 2 EAS.
Avanos Medical feeding tube These updated guidelines require users to check the placement of tubes according to the institution's protocols prior to using the tube.
Avanos Medical, based in Alpharetta Georgia, USA is a maker of clinical medical devices. The company's products are distributed in more than 90 countries.
Last December, the company entered into a $160 million deal to purchase OrthogenRx. Avanos Medical concluded the acquisition on 20th January.
feeding tube placement
Here's my website: https://odolbodol.shop/index.php?page=user&action=pub_profile&id=2111506
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