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Avanos Recalls FDA Class II After 23 Deaths Associated with the Device
The Avanos Medical Cortrak*2 Ental Access System was created to aid trained health care professionals in placing medically-approved feeding tubes in the small intestines of patients or stomachs. https://penzu.com/p/12ae6c47 There are 23 deaths linked to feeding tubes since the year 2015.

Patients have died and injuries due to misplacement of nasoenteric/nasogastric tube placement devices.

Cortrak 2 eternal access system Avanos Medical The recall will be used to change the labels on the device as well as the instruction and the intended use. https://controlc.com/ab3adb5b The updates will require users to ensure that the tube is placed as per the guidelines of their institution before using the tube to provide nutrients.

Patients may suffer serious injuries or even death in the event that a nasogastric tube, or nasoenteric tub has been incorrectly installed.

Avanos Medical has issued a recall notification stating that, since 2015, there have been 60 patient deaths and 23 injuries resulting from the wrong placement of the nasogastric tube. feeding tube placement https://mooc.elte.hu/eportfolios/1458894/Home/Avanos_Recalls_FDA_Class_II_after_23_Deaths_Involved_with_the_device Respiratory failure, pneumothorax perforation (a hole, in the stomach wall) and pneumonia were all reported.

On the 21st of March 2022 Avanos Medical issued a field correction notification to its customers who used these devices between January 2021 to January 2022. These instructions were included in the notification:

Use nasogastric or Nasoenteric tubs according to the policies of the institution.
Attach the pertinent field correction notice to the operator’s guide.
Avanos Health Medical asks that you return the acknowledgement form with the email notification https://site-9257320-4348-8224.mystrikingly.com/blog/cortrak-2-eas-of-avanos-medical-raises-patients-safety-bespins
Homepage: https://mooc.elte.hu/eportfolios/1458894/Home/Avanos_Recalls_FDA_Class_II_after_23_Deaths_Involved_with_the_device
     
 
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