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Cortrak 2 EAS of Avanos Medical Raises Patient Safety Risks
Cortrak2 from Avanos Medical – can patients feel safer? Maybe an New Report will reveal the answer.

Avanos Medical was one of the first manufacturers of Cortrak 2 Enteral Access System.

The Cortrak 2 is a device which allows you to put a feeding tube in the medical field.

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.

Among the 51 MDRs 11, 11 patients died due to misuses of the Cortrak 2 device.

Fox News just recently reported that Avanos Health had released an error-correction notice for Cortrak2EAS due to potential deadly results.

This case demonstrates the serious dangers of this business and the impact it has on health.

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

Avanos Medical was also charged criminally for fraud in branding.
The medical device industry is among the most regulated sectors globally because of the impact it has on the lives of humans.

In spite of these rules yet, there are many worrying cases in this sector.

Although the name 'Avanos' may not sound appealing, if your interest is in the field of medical devices you may have come across an instance of this company.

Avanos has sold thousands of MicroCool Sacrificial gowns in the months of November 2014-January 2015.

According to the company, MicroCool surgical garments were protected from virus and fluid penetration , as they met the highest standards of the FDA. However, this was false as the surgical gowns failed the viral penetration tests, and the company was modifying the method employed to seal the gowns.

feeding tube placement All this information was discovered in July 2016 by the FDA when it conducted an investigation of Avanosthe business that sold surgical gowns.

They found out that an employee forged company papers in order to deceive FDA.

Hundreds of people have been injured because of these defective and unsafe devices.

So if Avanos realized they were not able to prove that their MicroCool surgical gowns do not provide the best protection against the penetration of viruses and fluids, why did they make this claim, and then fake documents?

Keep in mind that medical fields can be a delicate one and numerous people have lost their lives as a result of their actions.

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

Avanos has signed an agreement on a voluntary basis with the Department of Justice to defer the prosecution of criminal offenses under the Federal Food, Drug & Cosmetic Act.

Avanos Mediacal Cortrak 2 Avanos continues to face issues with their products.

The FDA and DOJ have been cited numerous times for crimes related to their products. Despite the agencies efforts to address the issue, people continue experiencing issues with the company's products.

Patients must feel comfortable when using medical devices. Patients don't need to worry whether their medical device they use or their disease will cause death.

Avanos and other medical device firms pose a risk to the safety of patients if they are not exposed.

The criminal conduct of the company has been demonstrated in numerous cases. The company must be held accountable.

feeding tube placement Avnos Medical Issues: A field correction notice concerning the Cortrak 2 EAS

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

Similar to surgical gowns and feeding tube placement devices like Cortrak 2 Cortrak 2 can save lives.

Avanos Medical is suing to misbrand the MicroCool surgical gown. The lawsuit has raised questions about all medical devices manufactured by Avanos Medical.

Indeed the concerns were valid.

Avanos, as stated previously has released a free correction field for the Cortrak 2 EAS. That could have caused injury, death, or both.

Ironically Avanos Medical claims that its system eliminates such issues through screen visualization and location data in the process of tube placement. They can confirm their tube placement with the use of x-rays less frequently.

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

They claimed that they were "unable to provide a comment" and also stated that the FDA did not ask for recall.

When using medical devices like Cortrak 2, Cortrak 2, which have already raised cause for concern it is imperative to be extremely cautious.

It has been established that Cortrak 2 may severely cause injury or even risk patients' lives.

Despite the modifications that Avanos Medical claims to make changes to their manufacturing and medical device approval systems Patients and health professionals aren't able to know for sure that these products are safe.

Avanos Medical feeding tube Avanos Medical should be visited again by the FDA and Department of Justice to provide peace to patients and their families.
My Website: https://www.hpnonline.com/regulatory/article/21267840/fda-class-i-recall-cortrak2-enteral-access-system-by-avanos-medical