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Avanos Medical recalled Cortrak* 2 EAS in the wake of incidents of injury and patient deaths due to tube malfunctions.
https://mooc.elte.hu/eportfolios/372895/Home/Avanos_Recalls_Cortrak2_Over_Potential_Enteral_Tube_Misplacement The US Food and Drug Administration has recognized Avanos Medical's Cortrak*2 enal Access System Recall (EAS) as a Class I recall.
Cortrak 2 eternal access system The most dangerous of the three types is the Class I remember.
Avanos Medical pulled Cortrak* 2 EAS off service following patient deaths and injuries due to nasogastric tube misplacements.
This device can be used to assist trained health professionals with the placement of medical feeding tubes into patients. https://controlc.com/98350d7a It also provides real-time information about tube placement.
However, the wrong placement of the nasogastric, or nasoenteric tubes could result in severe injuries or even death.
The company has now removed 629 devices from the US that were distributed between April 1, 2016 and 1 January 2022.
Avanos Mediacal Cortrak 2 The company also stated in a recall communication that there were 60 injuries and 23 patients that died in 2015 as a result of the feed tubes that were not properly placed in the Cortrak* 2 EAS.
Avanos Medical, following the recall, will update the labeling of the device. This will include updating the instructions and intended uses for Cortrak* 2 EAS.
Users are also directed to confirm that the tubes have been put in the correct manner according to the guidelines of the institution before they use.
Avanos Medical, based in Alpharetta Georgia, USA, is a manufacturer of clinical medical devices. The company has more than 90 markets that are branded with its brands.
The company agreed to acquire OrthogenRx for $160 million in December. Avanos Medical concluded the acquisition on 20th January.
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Here's my website: https://canvas.instructure.com/eportfolios/1253644/Home/Cortrak_2_EAS_by_Avanos_Medical_Increases_Patient_Safety
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