Notes

Cortrak EAS 2 of Avanos Medical Causes Questions About Patient Safety
Cortrak Medsystems Cortrak 2 device.

11 patients of the 51 MDRs were killed due to misuse of Cortrak 2 devices.

Fox News reported that Avanos Medicine published an error announcement regarding Cortrak 2 EAS. The notice was issued due to fatalities that could have occurred.

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

Avanos Medical feeding tube The Food and Drug Administration might be looking into the matter.

Avanos Medical was not the only one to mess with the FDA. A criminal case was filed against the firm for fraud in branding.
The medical device industry is among the industries that are most controlled globally because of its impact on the lives of humans.

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

Although it might not sound like a huge deal however, the name Avanos Med might. If it is related to the medical device sector, you may have read about an intriguing case.

https://www.techtimes.com/articles/275216/20220509/cortrak-2-eas-from-avanos-medical-raises-patient-safety-concerns.htm Avanos sold thousands of MicroCool surgical clothing and misbranded them between November 2014 and January 2015.

They claimed that MicroCool surgical gowns met FDA's strictest standards and could prevent infection by viruses and fluids. However, this was not true as the surgical gowns failed tests for penetration of viruses and the firm was changing the methods used to seal these gowns.

The information was uncovered in the month of July by the FDA when it conducted an investigation of Avanosthe business that sold surgical gowns.

To fool FDA they discovered fraudulent company records which an employee had prepared.

Hundreds of people were injured due to these defective and poorly created devices.

Avanos knew that their MicroCool surgical gowns did not provide the best protection against the entry of virus and fluids. Why did they make such a claim, and even falsify documents?

Be aware that the medical field is extremely delicate. https://www.fiercebiotech.com/medtech/avanos-medical-faces-class-i-recall-feeding-tube-system-linked-23-deaths-2015 And who is aware of how many people were killed because of their conduct?

For more information about Avanos Medical, please call
Avanos Medical arranged to pay $22 million under an Data Processing Agreement.

Avanos reached a Deferred Prosecution agreement with the Department of Justice in relation to criminal violations of Federal Food, Drug & Cosmetic Act.

Avanos Mediacal Cortrak 2 Avanos is currently having issues with its products.

They have been fined repeatedly by the FDA as well as the DOJ for criminal activities associated with issues with their goods. Despite all of these efforts, many people still have problems with the products of the company.

Patients should feel comfortable making use of medical equipment. So they don’t have to be concerned about who will cause their death, whether it's the medical devices or their illness.

Avanos, the medical device manufacturer poses a danger for the health of patients in the event that they are not protected.

The company has been accused of criminal conduct in several cases. They must be held accountable.

Avnos Health Issues is a field correction announcement regarding the Cortrak 2 EAS

Avanos medical produces the Cortrak2 feeding tube.

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

The case regarding the misbranding of MicroCool surgical gowns by Avanos Medical has raised cause for concern about all medical devices produced by the company.

The concerns were true.

https://www.fda.gov/medical-devices/medical-device-recalls/avanos-medical-recalls-cortrak2-enteral-access-system-risk-misplaced-enteral-tubes-could-cause Avanos Medical feeding tube Avanos has issued an uninvoluntary correction to Cortrak 2 EAS. This could have led to injury or death.

Ironically, Avanos Medical claims it avoids these issues by using screen visualizations and location information when placing the tube. So, they'll have less need for the confirmation of x-rays.

Avanos confirmed that with Fox News they are in an "ongoing dialogue" with the FDA on the matter.

They claimed that they could not comment and added that the FDA has not requested to recall any product.

You must exercise care when using medical equipment such as Cortrak 2, that have already raised concerns.

It's been proven that Cortrak2 could severely injure or even threaten patient's lives.

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

The FDA and the Department of Justice should pay another visit to the Avanos Medical offices to reassure the patients and their families.
Website: https://www.fiercebiotech.com/medtech/avanos-medical-faces-class-i-recall-feeding-tube-system-linked-23-deaths-2015