Notes

Cortrak 2 EAS from Avanos Medical raises Patient Safety Concerns
Cortrak Medsystems Cortrak 2 device.

11 patients of the 51 MDRs were killed in the mishandling of Cortrak 2 devices.

Only recently, Fox News revealed that Avanos Medical published an error-in-field notice regarding its Cortrak 2 EAS due to the possibility of deadly outcomes.

Avanos Mediacal Cortrak 2 This is a stark warning of the dangers of feeding tubes and their impact on human life.

This revelation could lead to an investigation being conducted by the Food and Drug Administration (FDA).

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

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

While the name "Avanos Medical" may not be familiar, if you are a follower of the medical device industry you might have been aware of a situation with this company.

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

They claimed that the MicroCool surgical gowns could be protected from fluid and virus penetration and meet FDA's strictest standards. However, this is a lie since the gowns passed the tests for virus penetration. Furthermore, the company was changing the method used to seal the gowns.

They were all discovered after FDA investigators investigated Avanos' business in surgical gowns.

They discovered that an employee forged documents for the company in order to be deceived by FDA.

The devices were poorly constructed and defectively created and resulted in the deaths of hundreds of people.

If Avanos knew that their MicroCool surgical gowns were not safe from fluid and virus penetration So, what is the reason they claimed safety and falsely document their claims?

Remember that the medical industry is a delicate field. feeding tube placement And who is aware of how many people were killed because of their actions?

For more information about Avanos Medical, please call
Avanos Medical, in July 2021, signed an agreement to pay $22,000,000 as part of a Data Processing Agreement. (DPA). The agreement was made to end the felony charge.

Avanos entered into a deferred prosecution agreement with the Department of Justice regarding criminal violations of the Federal Food, Drug & Cosmetic Act (FDCA).

Avanos is currently having issues in its products.

Several times they have been penalized by the FDA and the DOJ for criminal activities connected to their products. Despite the agencies efforts however, some people are still having problems with their products.

Patients need to feel secure using medical devices. They don't have worry about whether their medical device or illness could kill them.

Avanos as well as other medical device companies pose a risk to the safety of patients, if they're not exposed.

This company has shown the worst of behavior in a variety of instances. https://www.transtats.bts.gov/exit.asp?url=https://www.rheingoldlaw.com/blog/2022/may/avanos-faces-fda-class-i-recall-after-23-deaths-/ It is required to be held accountable for its actions.

Avanos Medical Avnos Medical issues a corrections notice regarding Cortrak 2 EAS

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

Avanos Medical feeding tube Cortrak 2 eternal access system As with dressing gowns for surgery and devices to place feeding tubes, such as the Cortrak 2, are vital in saving lives.

Avanos Medical's misbranding case of MicroCool surgical dresses has caused worry about all medical equipment manufactured by the company.

The concerns raised were valid.

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

It's ironic the fact that Avanos Medical claims that their method eliminates these issues through the use of location information and visualizing the screen during tube's placement. They are able to verify the tube's placement using scans of the x-rays more frequently.

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

They stated that they were "unable to comment" and stated that the FDA didn't request recalls.

If you are using medical devices, like the Cortrak 2, which have been a source of concern There is a need for extreme caution.

It has been proven that Cortrak2 may cause serious injuries to and even kill patients.

Avanos Medical claims that they have made improvements to the development of medical devices approval systems. However, it's impossible for consumers or health professionals to be certain that these products are safe. actually are.

Avanos Medical offices should be visited by the FDA as well as the Department of Justice in order to ensure the safety of patients and their families.
Website: https://www.transtats.bts.gov/exit.asp?url=https://www.rheingoldlaw.com/blog/2022/may/avanos-faces-fda-class-i-recall-after-23-deaths-/