Notes

Cortrak 2 EAS from Avanos Medical raises Safety of Patients
Cortrak Medsystems Cortrak 2 device.

Among the 51 MDRs 11, 11 patients died as a result of mistakes made with the Cortrak 2 device.

Fox News just recently reported that Avanos Health had released an error-correction notice for Cortrak2EAS due to possible fatal consequences.

Avanos Medical feeding tube This is an eloquent reminder of the dangers of the industry that fuels the tube and its effect on the lives of the people.

The Food and Drug Administration could be examined.

Avanos Medical was not the first company to make a mistake with the FDA.
Avanos Medical Due to its direct effect on the lives of humans The medical device industry is among the industries that is most tightly controlled.

However, there are worrying cases in the industry despite these regulations.

While the title "Avanos Medical" may not be a familiar one If you're an avid follower of medical device industry you might have heard about a case with this company.

Avanos Medical Avanos sold hundreds and thousands of MicroCool surgical dresses from November 2014 until January 2015.

According to them they claimed that according to them, the MicroCool surgical gowns met the highest standard established by the FDA and effectively protected against virus and fluid penetration. The claim was bogus since the gowns failed to pass the viral penetration tests and the company was modifying the method of sealing gowns.

All this information was discovered in July 2016 by the FDA when it investigated Avanos’ business selling surgical gowns.

They found out that an employee falsified documents of the company to be deceived by FDA.

These devices that were poorly designed resulted in the injury of hundreds.

Avanos should have known that MicroCool's surgical gowns were not the safest against the spread of viruses. However, they claimed they were and falsified documents.

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

Call for further scrutiny into Avanos Medical
Avanos Medical arranged to pay $22 Million under a Data Processing Agreement.

Avanos signed an agreement to defer prosecution (DPA) with the Department of Justice for criminal violations of Federal Food, Drug & Cosmetic Act.

Avanos continues to have problems with their products.

Several times they have been cited by the FDA and the DOJ for criminal acts related to issues with their goods. Cortrak 2 eternal access system Despite all of these agencies' efforts, a few are still experiencing issues with their products.

Patients must be comfortable with medical devices. Patients don't need to worry whether the medical device or their illness will kill them.

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

https://www.medicaltubingandextrusion.com/avanos-medical-recall-of-cortrak-2-enteral-access-system-is-class-i/ The company is accused of committing crimes in numerous instances. They are required to be held accountable.

Avnos Medical Issues a field correction notice about the Cortrak 2 EAS

As stated earlier, Avanos medical is responsible for the manufacturing of the Cortrak 2 feeding tube device.

Like surgical gowns and feeding tube placement devices like Cortrak 2, Cortrak 2, are vital in 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.

In fact, these issues were legitimate.

Avanos has, as previously reported, released a voluntary correction field to the Cortrak 2 EAS. That could have resulted in injury, death, or both.

Ironically, Avanos Medical claims it avoids these problems with screen visualizations and information about location during tube placement. They don't need x-ray confirmation.

Fox News interviewed Avanos to confirm that they are in an ongoing dialogue with FDA on this issue.

Cortrak 2 eternal access system They said they "cannot comment" regarding the issue and also stated that the FDA hasn't asked for a recall of products.

When using medical devices such as Cortrak 2, Cortrak 2, which have been a source of concern it is imperative for great caution.

Cortrak 2 eternal access system It has been proven that Cortrak 2 may severely harm or even threaten patients' lives.

Avanos Medical may have made some changes in the production process and approval of medical devices however it's still not enough to guarantee the safety of patients and other health professionals.

Avanos Medical offices should be visited by the FDA along with the Department of Justice in order to provide comfort for patients and their families.
My Website: https://casereports.bmj.com/content/2016/bcr-2016-216738