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Cortrak 2 EAS from Avanos Medic Increases Patient Safety
Cortrak 2, produced by Avanos Medical, - Can the patients feel safe? New Report may reveal the answer

Avanos Medical, one of the Cortrak 2 Enteral Access System manufacturers (EAS), is also known as Avanos Medical.

Cortrak 2 is a feeding tube device used in medicine.

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.

One of the 51 MDRs died from misuse of the Cortrak 2 device.

Fox News recently revealed that Avanos medical published the field correction notes for its Cortrak2 EAS. Avanos Medical feeding tube This could have been due to deadly outcomes.

https://recalls-rappels.canada.ca/en/alert-recall/cortrak-2-enteral-access-system This highlights the serious dangers of feeding tubes and their impact on human life.

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

Avanos Medical was not the only company to tamper with the FDA. A criminal charge was filed against the firm for fraud in misbranding.
Because of its effect on human life Medical device manufacturing ranks among the most tightly monitored industries around the globe.

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

Although the title "Avanos Medical" may not be familiar, if you are an avid reader of medical device industry news you might have been aware of a situation with the company.

Avanos sold hundreds of MicroCool surgical gowns between November 2014 and January 2015.

They stated that MicroCool surgical dresses met the FDA's standards for the highest quality and could prevent the spread of viruses and fluids. But, this assertion was a lie since the gowns for surgery failed tests of penetration by viruses, and the firm was modifying the sealing methods used to seal these gowns.

The information was uncovered in July 2016 by the FDA when it conducted an investigation of Avanoscompany that sells surgical gowns.

They found falsified company documents that were created by an employee of the company in order to deceive FDA.

These devices that were not of high-quality resulted in hundreds of injuries.

In other words, if Avanos was aware they were not able to prove that their MicroCool surgical gowns do not provide the best protection against the penetration of viruses and fluids So why did they put forward this claim, and then fake documents?

Remember, the medical profession is delicate, and who knows how many people died due to their actions.

Demand further investigation into Avanos Medical
In July 2021 Avanos Medical agreed to pay $22 million as part of a Data Processing Agreement (DPA) to end this felony.

Avanos and the Department of Justice reached a deferred prosecution arrangement regarding criminal violations of Federal Food, Drug & Cosmetic Acts (FDCA).

Avanos's products have caused issues for many years.

Several times they have been cited by the FDA and the DOJ for criminal activity connected to their goods. Even with the best efforts made by agencies, some people still have issues with the company’s products.

Patients must feel comfortable using medical equipment. Avanos Medical Patients don't need to worry whether their medical device or disease will cause death.

Avanos, an medical device manufacturer, poses a danger for the health of patients when they're not in contact with it.

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

Avnos Medical issue a correction notice for Cortrak 2 EAS

Avanos medical produces the Cortrak2 feeding tube.

As surgical gowns do, feeding tube placing devices such as the Cortrak 2 can save lives.

Avanos Medical misbranded the MicroCool surgical dressings, causing concern about all medical devices manufactured by the company's management.

Avanos Mediacal Cortrak 2 The concerns were valid.

https://www.fdanews.com/articles/207866-avanos-medical-gets-class-i-designation-for-its-recalled-cortrak2-enteral-access-system As we mentioned earlier, Avanos released a voluntary correction to the field for the crucial Cortrak 2 EAS, that could have resulted in injury or even death.

Incredibly, Avanos Medical claims that its system will eliminate these issues by using visualizing the screen and storing location information when placing the tube. This allows them to eliminate the need for xray confirmation.

Fox News reported that Avanos confirmed in a conversation with Fox News that they are currently engaged in an "ongoing discussion" with FDA concerning the matter.

They said they "cannot speak" on the subject and also stated that the FDA hasn't yet requested recalls of products.

If you are using medical devices, like the Cortrak 2, which have already raised cause for concern it is imperative for great caution.

It has been shown that Cortrak 2 can seriously harm and end the lives of patients.

Avanos Medical claims they have improved their manufacturing and approval process, however, healthcare professionals and patients aren't able to determine the level of safety these products are.

The FDA and the Department of Justice should pay another visit to Avanos Medical's offices to assure the patients and their families.
Read More: https://recalls-rappels.canada.ca/en/alert-recall/cortrak-2-enteral-access-system