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Cortrak EAS 2 of Avanos Medical Raises Beserks Concerns about Patient Safety
Cortrak 2 from Avanos Medical: Can patients feel safe? New Report could reveal the solution

Avanos Medical is one of the producers of the Cortrak 2 Enteral Access System (EAS).

Cortrak 2 devices are used in medical fields to place feeding tubes.

Between January 2012 to July 2017, the FDA received 51 Medical Device Reports (MDRs) about pneumothorax events related to the Cortrak Medsystems Cortrak 2 device.

11 MDRs among 51 died due to misusing the Cortrak 2 unit.

Avanos Medical Fox News recently revealed that Avanos medical issued a field correction note regarding its Cortrak2 EAS. This was due to the possibility of deadly outcomes.

This is a stark warning of the dangers of feeding tubes as well as the effects they have on human lives.

This could result in an investigation being conducted by Food and Drug Administration.

Avanos Medical was not the first to brand the FDA in a different way. FDA.
Due to its influence on human lives, the medical device industry is among the most tightly controlled industries in the world.

Despite all the regulations however, there's an abundance of concerns in the industry.

The name 'Avanos medical' might not ring a bell, but if you follow the news in the field of medical devices it is possible that you have heard of a story concerning the company.

Between November 2014 to January 2015, Avanos sold hundreds of thousands of fake MicroCool surgical gowns.

According to MicroCool, its surgical gowns meet the FDA's highest standards for protection against viruses and fluids. But, this assertion was not true as the surgical gowns failed tests of penetration by viruses, and the company was altering the sealing methods used to seal these gowns.

The whole story was exposed when FDA investigated Avanos"surgeon's gown business.

The FDA was deceived by false company documents that were created by an employee of the company.

Cortrak 2 eternal access system The devices' design flaws led to the injuries of hundreds.

Avanos was aware that their MicroCool surgical gowns did not provide the greatest safety against entry of viruses and fluids. Why did they make such a claim? And even falsify documents?

Keep in mind that the medical field is not a safe profession. It is impossible to know how many lives affected by their actions.

Avanos Mediacal Cortrak 2 Avanos Medical is available for consultation
In July 2021, Avanos Medical agreed to pay $22 million as part of a Data Processing Agreement (DPA) to settle this felony charge.

Avanos Medical Avanos signed a deferred prosecution agreement (DPA) with the Department of Justice for criminal violations of Federal Food, Drug & Cosmetic Act.

At this point, Avanos has repeatedly had issues with their products.

Numerous times, they've been penalized by the FDA and the DOJ for criminal activities connected to their products. https://www.massdevice.com/avanos-medical-recall-of-cortrak-2-enteral-access-system-is-class-i/ Despite the efforts of the agencies, there are many who have issues with the company’s products.

Patients should feel comfortable using medical devices. They don't have worry about whether their medical device or illness will kill them.

Avanos and other medical device companies pose risks to the safety of patients if they aren't exposed.

In several instances the company exhibited an act of criminality and should be held responsible.

Avnos Medical issues a correction notice for Cortrak 2 EAS

Avanos medical, as previously mentioned, is the company responsible for the production of the Cortrak 2 feeding tube.

As with surgical gowns and feeding tube placement devices like the Cortrak 2, are vital in saving lives.

Avanos Medical is suing to misbrand the MicroCool surgical dressing. This has raised concerns about all medical devices manufactured by Avanos Medical.

Indeed, these concerns were right.

Avanos issued an uninvoluntary correction to Cortrak 2 EAS. This could have led to injury or death.

Incredibly, Avanos Medical claims that its system eliminates such issues through screen visualization and location data in the process of tube placement. They don't need x-ray confirmation.

Avanos confirmed in an interview with Fox News they are in an "ongoing dialogue" with the FDA regarding the issue.

They claimed they were unable to make a statement, and that the FDA hadn't asked them to recall any product.

There is a need to be careful when using medical devices such as Cortrak 2. Cortrak 2, which has been a source of concern for a while.

It has been demonstrated that Cortrak 2 may severely harm or even threaten the lives of patients.

Avanos Medical claims they have made significant improvements in their manufacturing and medical device approval process, however, patients and health professionals aren't able to determine the level of safety these products are.

Avanos Mediacal Cortrak 2 Avanos Medical should be visited time and time again by the FDA and Department of Justice to provide peace to patients and their families.
Read More: https://www.fdanews.com/articles/207866-avanos-medical-gets-class-i-designation-for-its-recalled-cortrak2-enteral-access-system?v=preview