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Cortrak 2 EAS by Avanos Medical Boosts Patient Safety
Cortrak 2 by Avanos Medical - can the patients feel secure? The answer might be found in a recent report

Avanos Medical, one of the Cortrak 2 Enteral Access System manufacturers (EAS), is also known as Avanos Medical.

The Cortrak 2 device, a feeding tube placing device, is utilized in the medical industry.

Between January 2012 to July 2017, the FDA received 51 Medical Device Reports (MDRs) about pneumothorax events related to the Cortrak Medsystems Cortrak 2 device.

11 MDRs of the 51 who died because of misuse of the Cortrak 2 unit.

Fox News reported that Avanos Medicine published a correction announcement for Cortrak 2 EAS. The notice was released in response to possible fatalities.

Avanos Medical This incident highlights the risks of the feed tube business as well as the effects it has on the lives of people.

The news could trigger the Food and Drug Administration (FDA) investigation.

Avanos Medical was also charged with fraud for misbranding.
The industry of medical devices is one of the most regulated sectors globally due to its effect on human lives.

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

Avanos Medical feeding tube Although the name "Avanos Medical" may not be a familiar one but if you're an avid reader of medical device industry, you may have read about a controversy with this company.

From November 2014 until January 2015, Avanos sold hundreds of thousands of fake MicroCool surgical gowns.

According to them they claimed that the MicroCool surgical gowns met the strictest standards that was set by the FDA and could effectively protect against the penetration of viruses and fluids. This claim was false, as the surgical gowns failed the tests to determine the penetration of viruses and the firm was modifying the way they sealed the gowns.

The information was uncovered in July 2016 by the FDA when it investigated Avanosthe business that sold surgical gowns.

To deceive FDA they found fraudulent company records which an employee had prepared.

The devices were poorly constructed and manufactured in a way that was defective and resulted in the deaths of hundreds of people.

Avanos probably knew they were not the best MicroCool gowns they created for surgical purposes did not offer maximum protection against virus and fluid penetration. Why did they claim this?

Remember that the medical profession is delicate. It is impossible to know how many lives were affected by their actions.

Contact Avanos Medical for more information
Avanos Medical arranged to pay $22 million under an 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 has continued to experience problems with its products.

The FDA and DOJ have issued citations to them numerous times for crimes related to their products. Avanos Medical feeding tube Despite all these efforts, people continue to have problems with the products of the company.

https://biotech-insider.com/avanos-medical-faces-class-i-recall-for-feeding-tube-system-linked-to-23-deaths-since-2015/ Patients should feel secure while using medical devices. In order to not be concerned about what could kill them, the medical device, or even their illness.

Avanos as well as other medical device makers, pose a threat for patients' safety.

The company has displayed the same criminal behavior in multiple instances and must be held responsible for its actions.

Avnos Medical Issues A field correction notification regarding the Cortrak 2 EAS

Avanos Medical is responsible for the production of Cortrak 2's feed tube.

Like surgical gowns, feeding tube placing devices like Cortrak 2 Cortrak 2 can save lives.

Cortrak 2 eternal access system Avanos Medical is suing to falsely brand the MicroCool surgical dressing. The lawsuit has raised questions regarding all medical products made by Avanos Medical.

Avanos Medical The issues were legitimate.

As stated before, Avanos released a voluntary field correction for the crucial Cortrak 2 EAS, that could have caused the death or injury of.

In a way, Avanos Medical claims its system will help avoid these issues with screen visualization and location information during tube placement. It doesn't require confirmation by x-ray.

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

They claimed that they "cannot make any comments" regarding the issue and also stated that the FDA hasn't asked for a recall of the products.

There is need to be cautious with medical devices such as Cortrak 2. Cortrak 2, which has already raised questions.

It's been demonstrated that Cortrak2 can seriously injure or even threaten patient's lives.

Avanos Medical claims they have made substantial improvements to their manufacturing and approval procedures, however, patients and health professionals aren't able to determine how safe these devices are.

The FDA and the Department of Justice should pay another visit to the offices of Avanos Medical to assure the patients and their families.
Read More: https://biotech-insider.com/avanos-medical-faces-class-i-recall-for-feeding-tube-system-linked-to-23-deaths-since-2015/