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Cortrak 2 EAS of Avanos Medical Raising Patient Safety Issues
Cortrak Medsystems Cortrak 2 device.

One of the 51 MDRs died from abuse of the Cortrak 2 device.

Fox News has just revealed that Avanos Med issued a field correct notice regarding Cortrak2 EAS. It was to prevent potential fatal consequences.

This incident highlights the dangers of the feed tube industry and its impact on people's lives.

The Food and Drug Administration could be studied.

Avanos Medical was also charged criminally for fraudulent misbranding.
Due to its direct impact on human lives The medical device industry is one of the industries that is most tightly controlled.

Despite all the regulations however, there's a lot of concern within the field.

The name "Avanos Medical" may not sound like a ringing bell, but if you keep an eye on the news in the field of medical devices, you might have heard of a story regarding this company.

Avanos Mediacal Cortrak 2 Avanos sold thousands of MicroCool surgical gowns between November 2014 and January 2015.

According to MicroCool's website, the surgical gowns meet FDA's highest standards for protection from viruses and fluids. But, this assertion is false since the surgical gowns failed the virus penetration tests. Additionally the company was altering the method of sealing the gowns.

All of these were discovered by FDA inspectors in July of 2016, as they conducted an investigation of Avanossurgical gowns' business.

https://www.mpo-mag.com/contents/view_breaking-news/2022-05-16/avanos-recalls-cortrak2-over-potential-enteral-tube-misplacement The FDA was deceived through falsified company documents , which were drafted by an employee of the firm.

These poor-quality devices led to hundreds of injuries.

Avanos ought to have realized that MicroCool's surgical gowns were not the best protection against the spread of viruses. https://www.fdanews.com/articles/203704-avanos-medical-to-pay-22-million-settlement-over-misbranded-surgical-gowns They claimed that they were and forged documents.

Be aware that medical professionals are fragile and many lives were lost as a result of their actions.

Contact Avanos Medical for more information
Avanos Medical made a $22 million payment as a part of a Data Processing Agreement.

Avanos reached a Deferred Prosecution agreement with the Department of Justice in relation to criminal violations of the Federal Food, Drug & Cosmetic Act.

At this point, Avanos has repeatedly had issues with its products.

Many times, they've been mentioned by the FDA and the DOJ for criminal activity in connection with issues with their products. Despite the best efforts of authorities there are still some who have problems with the company's products.

Patients must feel comfortable when using medical devices. Therefore, they won't have to worry about what might end their life first - the medical device or their condition?

Avanos and other medical device companies could pose a risk to patient safety if disclosed.

The company has shown pattern of criminal conduct in several instances and must be held accountable for its conduct.

Avnos Health Issues is a field correction notification regarding the Cortrak 2 EAS

Avanos is the manufacturer of the Cortrak2 feed tube.

Like dressing gowns for surgery and devices to place feeding tubes, such as Cortrak 2, Cortrak 2, are vital in saving lives.

There has been concern about the medical devices manufactured by Avanos Medical because of the incorrect branding of MicroCool surgical gowns.

The concerns were true.

Avanos was able to make a voluntary field correction to the Cortrak 2 EAS. It could have led to injuries or even death.

It's ironic that Avanos Medical claims their system prevents these issues by using screen visualization and location information for the placement of the tube. They can do this without having to get x-ray confirmation.

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

Avanos Medical feeding tube They said they "cannot make any comments" and stated that the FDA has not asked to conduct a product recall.

https://www.fda.gov/medical-devices/medical-device-recalls/avanos-medical-recalls-cortrak2-enteral-access-system-risk-misplaced-enteral-tubes-could-cause It is important to exercise extreme caution when using medical equipment such as Cortrak 2, that have already raised concerns.

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

Despite the improvements which Avanos Medical claims to make to their production and approval of medical devices Patients and health professionals cannot be certain of that these products are safe.

Avanos Medical offices should be visited by the FDA along with the Department of Justice in order to provide comfort for the families of patients.
Here's my website: https://www.medicaldevice-network.com/news/fda-avanos-medical-cortrak2-eas-recall/