Notes

Cortrak 2 EAS of Avanos Medical Raising Patient Safety Issues
Cortrak Medsystems Cortrak 2 device.

Avanos Mediacal Cortrak 2 The 11 victims were part of 51 MDRs who died because from the misuse of Cortrak 2.

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

This incident highlights the serious dangers of the feeding tube industry and its effect on lives of individuals.

The Food and Drug Administration might be conducting an investigation into the incident.

Avanos Medical was not the first to make a mistake with the FDA.
The effect of medical devices human life is what makes it one of the most regulated industries worldwide.

Despite these laws however, there are many worrying cases in this industry.

Although the name "Avanos medical" may not immediately obvious, it's possible that you've been watching the news about the medical devices industry to learn about a case about this company.

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

They stated that MicroCool surgical gowns met FDA's standards for the highest quality and could prevent the spread of viruses and fluids. The company had to change the sealing techniques and did not pass the viral penetration test therefore this claim was not accurate.

All of them were discovered when FDA investigators looked into Avanos company in surgical gowns.

Avanos Medical To fool FDA to deceive FDA, they discovered falsified documents issued by the company.

These devices that were defective caused injuries to hundreds.

Cortrak 2 eternal access system So if Avanos was aware they were not able to prove that their MicroCool surgical gowns do not offer the greatest protection against the penetration of viruses and fluids So why did they put forward such a claim and even fake documents?

Rememberthat the medical profession is a delicate one and it is hard to know how many people died as a result of their actions.

Demand further investigation into Avanos Medical
Avanos Medical, in July 2021, agreed to make a payment of $22,000,000 as part of an Data Processing Agreement. (DPA). The agreement was made to end this felony conviction.

Avanos has entered into an agreement on a voluntary basis with the Department of Justice to defer the prosecution of criminal offenses under the Federal Food, Drug & Cosmetic Act.

Avanos has faced numerous issues with its products up to this point.

They have been fined multiple times by both the FDA and DOJ for criminal activity related with issues with their goods. Despite all these agencies' efforts, a few are still experiencing issues with the products of the company.

feeding tube placement Patients need to feel safe while using medical devices. Patients don't need to worry whether their medical device or their illness could kill them.

If not exposed medical device companies such as Avanos can pose a threat to the health of patients.

In multiple cases the company exhibited unacceptable behavior, and must be held responsible.

Avnos Medical Issues A field correction notice concerning the Cortrak 2 EAS

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

Like surgical gowns but with feeding tubes, equipment such as the Cortrak 2 that place feeding tubes are vital to saving lives.

Avanos Medical misbranded the MicroCool surgical dressings, which has raised concerns about the quality of all medical devices produced under the control of the company.

These concerns are indeed valid.

Avanos performed an error in the field that was made by the Cortrak 2 EAS. It could have led to injury or even death.

In a way, Avanos Medical claims their system can prevent these problems by using screen-based visualization and location information for the placement of the tube. They are able to confirm the placement of their tube using x-rays less often.

Fox News confirmed that Avanos and the FDA are engaged in "ongoing dialogue" regarding the matter.

They claimed that they were unable to comment, and added that the FDA did not have asked to recall any products.

You should exercise great care when using medical equipment such as Cortrak 2, that have already raised questions.

It's been demonstrated that Cortrak2 can seriously injure or even threaten the lives of patients.

Despite the improvements which Avanos Medical claims to make in their production process and approval of medical devices, patients and health professionals aren't able to know for sure how safe these products are.

The Avanos Medical offices must be checked out by the FDA as well as the Department of Justice. This will assist in reassuring patients and their families.
Read More: https://www.techtimes.com/articles/275216/20220509/cortrak-2-eas-from-avanos-medical-raises-patient-safety-concerns.htm