Notes

Cortrak 2 EAS from Avanos Medical Raises Patients Safety Concerns
Cortrak Medsystems Cortrak 2 device.

One of the 51 MDRs died due to the misusing the Cortrak 2 device.

Fox News just recently reported that Avanos Health had published a Field Correction Notice for Cortrak2EAS due to the possibility of deadly outcomes.

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

This information could trigger an investigation by the Food and Drug Administration (FDA).

Avanos Medical was not the only company to tamper with the FDA. A criminal case was filed against the company for fraud in branding.
Due to its influence on human lives The medical device industry is one of the most rigorously controlled industries in the world.

Despite the stringent regulations there are still a few worrying cases.

While the name "Avanos Medical" might not sound familiar If you're an avid follower of medical device industry, you may have been aware of a situation involving this company.

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

They said that MicroCool surgical gowns meet the FDA's standards for the highest quality and could prevent infection by viruses and fluids. This assertion was not true since the gowns failed to pass the tests to determine the penetration of viruses and the company was modifying the method of sealing gowns.

These were all discovered when FDA investigators investigated Avanos company in surgical gowns.

To deceive FDA, they found falsified documents issued by the company.

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

If Avanos were aware that their MicroCool surgical gowns weren't safe from fluid and virus penetration, then what is the reason they claimed safety and falsely document their claims?

Keep in mind that the medical profession is extremely delicate. And who can tell how many patients were killed due to their actions?

Avanos Medical can be reached for more details
In July 2021, Avanos Medical agreed to pay $22 million in the context of an Data Processing Agreement (DPA) to end this felony.

Cortrak 2 eternal access system Avanos signed an agreement to defer prosecution with the Department of Justice regarding criminal violations of the Federal Food, Drug & Cosmetic Act (FDCA).

Avanos Medical Avanos continues to have problems with their products.

Many times, they were repeatedly cited by FDA and DOJ for criminal activity in connection with issues with their products. Despite these agency efforts, a few still experience problems with the products of the company.

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

Avanos Medical Avanos as well as other medical devices firms pose a risk to the safety of patients if they are not made aware.

The company's criminal actions have been proven in numerous instances. The company should be held responsible.

Avnos Medical Issues A field correction notice with regard to the Cortrak 2 EAS

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

As surgical gowns do and feeding tube placement devices such as Cortrak 2 Cortrak 2 can save lives.

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

Indeed, the concerns were correct.

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

Cortrak 2 eternal access system It's ironic that Avanos Medical claims its system will help avoid these issues with screen visualization and location information during tube placement. This allows them to avoid the requirement for xray confirmation.

Fox News confirmed that Avanos and the FDA are in "ongoing dialogue" concerning the issue.

They said they were unable to comment, and stated that the FDA has not requested to recall any product.

It is important to exercise extreme care when you use medical equipment such as Cortrak 2, that have already raised concerns.

It has been proven that Cortrak 2 may seriously harm and put an end to the lives of patients.

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

Avanos Mediacal Cortrak 2 Avanos Medical offices should be visited by the FDA along with the Department of Justice in order to ensure the safety of the families of patients.
My Website: https://www.mpo-mag.com/contents/view_breaking-news/2022-05-16/avanos-recalls-cortrak2-over-potential-enteral-tube-misplacement/