Essure is a small flexible coil made of a nickel-titanium alloy that is inserted into the fallopian tubes. Scar tissue forms around the device, creating a barrier that blocks sperm from reaching the eggs. The device was approved by the FDA for the U.S. market in 2002 and is currently manufactured by Bayer Healthcare.

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We know how devastating it can be when a medical device that you count on fails. Bayer Healthcare promoted the Essure contraceptive device to be a safe and effective alternative to other permanent birth control procedures. Yet thousands of women are struggling with the serious side effects and severe complications associated with this implant device.

Our attorneys have a proven track record of fighting negligent medical device manufacturers and securing our clients the most compensation available. We will do the same for you. If you have suffered a serious side-effect or severe complication from the Essure birth control implant device, contact us today. We are aggressive advocates for those harmed by the medical devices they trust, and we fight to get you the compensation you deserve.

If you are ready to let us help you get the compensation you deserve, fill out all fields of the form above. We'll help you get justice. No fees unless damages are collected.

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Complications from Essure? If you would like to learn more about your legal rights and options, call 832-690-4053 or complete the form below.  
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Attorney Advertising Disclaimer: The information you obtain at this site is not, nor is it intended to be, legal advice. You should consult an attorney for advice regarding your individual situation. We invite you to contact us and welcome your calls, letters and electronic mail. Contacting us does not create an attorney-client relationship. Please do not send any confidential information to us until such time as an attorney-client relationship has been established. Prior results do not guarantee a similar outcome. Pulaski Law Firm, PLLC, 2925 Richmond Avenue, Suite 1725, Houston, TX 77098 










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IVC Filter Lawsuit

IVC Filter Shards Can Strike the Lungs, Heart, or Brain.

An inferior vena cava (IVC) filter is a medical device made of wire that looks somewhat like a spider. IVC filter devices are implanted in the body’s largest vein. The device is intended to serve as an alternative to blood thinners / anticoagulant medications. An IVC filter is designed to capture blood clots. Some IVC filters are permanent, while others are retrievable and have the option to be removed.

If you have an IVC filter from 2003 and up, you may be entitled to financial compensation by filing an IVC filter lawsuit. Even if you do not have a complication, but have an IVC Filter, we encourage you to contact us using the form above.

Bayer Healthcare knew of the adverse events including device migration and organ perforation, and actively concealed them

The Essure device was improperly designed

The device can break after implantation 

Bayer misrepresented the safety and efficacy of the device

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Have You Suffered Serious Complications from the Essure Birth Control Implant?

Essure birth control device was promoted as a non-surgical, permanent birth control solution. However, the device has been associated with severe side effects including:

> Ectopic pregnancy, pregnancy, and miscarriage  

> Uterus and organ perforation

> Device migration into the abdomen or pelvic cavity

> Chronic pain

> Vaginal infection

> Allergic reaction/vaginal infection

> Heavy menstrual bleeding

These side effects can result in:

> Death

Hysterectomy

Complications from the Essure device are migration and perforation of the fallopian tubes, which can puncture the uterus and other nearby organs as it travels down through abdomen into the pelvic cavity.

The Most-Profitable Drug in America has Been Linked to Gambling & Sex Addiction. If You Have Been Affected, Financial Compensation May Be Available.

Attorney Advertising Disclaimer: The information you obtain at this site is not, nor is it intended to be, legal advice. You should consult an attorney for advice regarding your individual situation. We invite you to contact us and welcome your calls, letters and electronic mail. Contacting us does not create an attorney-client relationship. Please do not send any confidential information to us until such time as an attorney-client relationship has been established. Prior results do not guarantee a similar outcome. Pulaski Law Firm, PLLC, 2925 Richmond Avenue, Suite 1725, Houston, TX 77098

Let us help you get justice and compensation deserved. No fees unless damages are collected.

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More than 26,000 adverse event reports have been filed with the FDA over the severe side effects and devastating complications of the Essure device.

ESSURE BIRTH CONTROL DEVICE

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Thousands of Essure Adverse Events Reported

More than 26,000 adverse event reports have been filed with the FDA over the severe side effects and devastating complications of the Essure device. Some of these complications include:

> Allergic reactions to device metal components

> Heavy bleeding and irregular periods

Chronic pain, fatigue, and depression

> Bloating, headaches, weight gain, and hair loss

Study warns that patients who use PPIs are 20 percent to 50 percent more likely to develop CKD than non-users and of those who do use these drugs.*

Have You Suffered Serious Complications from the Essure Birth Control Implant?

Essure birth control device was promoted as a non-surgical, permanent birth control solution. However, the device has been associated with severe side effects including:  

Ectopic pregnancy, pregnancy, and miscarriage  

Uterus and organ perforation  I

Device migration into the abdomen or pelvic cavity

Chronic pain

Vaginal infection

Allergic reaction/vaginal infection

Heavy menstrual bleeding

These side effects can result in:

Death

Hysterectomy

Fallopian tube removal (Salpingectomy)

Get Help Now

How Bad is It?

Other women complained of device migration and perforation, saying that the device can move from the fallopian tubes, puncture the uterus and other nearby organs as it travels down through abdomen into the pelvis.

These adverse events and serious side effects can be so severe that women are forced to undergo complex retrieval surgery to have the device removed or must undergo a hysterectomy in an effort to get relief from the debilitating device complications.

Thousands of women are claiming that Bayer Healthcare knew of the dangers of the device and concealed these dangers from the FDA, the healthcare community, and from the women who had them implanted.

More than 26,000 adverse event reports have been filed with the FDA over the severe side effects and devastating complications of the Essure device inculding:

ESSURE BIRTH CONTROL DEVICE LAWSUIT

If you received the Essure birth control device and suffered serious side effects and complications, you may be eligible for compensation.

 CLAIMS           DENIALS          APPEALS

 

How Bad is It?

Other women complained of device migration and perforation, saying that the device can move from the fallopian tubes, puncturing the uterus and other nearby organs as it travels down through abdomen into the pelvic cavity.

These adverse events and serious side effects can be so severe that women are forced to undergo complex retrieval surgery to have the device removed or must undergo a hysterectomy in an effort to get relief from the debilitating device complications.

These side effects can be so severe that women are forced to undergo complex retrieval surgery to have the device removed via a hysterectomy or a salpingectomy in an effort to get relief from the debilitating device complications.

 

We are currently investigating claims that:

 CLAIMS           DENIALS         APPEALS

Women with Essure Face High Risk of Surgical Removal

With so many complaints being filed, researchers studied the effects of the Essure birth control device and reported in the October 2015 British Medical Journal that women who are implanted with the contraceptive were ten-times more likely to have to undergo re-operation than those who had their tubes tied. *Source

We are currently investigating claims that:

> Bayer Healthcare knew of the adverse events including device migration and organ perforation, and actively concealed them

> The Essure device was improperly designed

> The device can break after implantation

> Bayer misrepresented the safety and efficacy of the device

Complications from the Essure device are migration and perforation of the fallopian tubes, which can puncture the uterus and other nearby organs as it travels down through abdomen into the pelvic cavity.

CLAIMS

APPEALS

DENIALS

 

Thousands of Essure Adverse Events Reported

More than 26,000 adverse event reports have been filed with the FDA over the severe side effects and devastating complications of the Essure device. Some of these complications include:

Allergic reactions to device metal components

Heavy bleeding and irregular periodsI

Chronic pain, fatigue, and depression

Bloating, headaches, weight gain, and hair loss

 

 

Women with Essure Face High Risk of Surgical Removal

With so many complaints being filed, researchers studied the effects of the Essure birth control device and reported in the October 2015 British Medical Journal that women who are implanted with the contraceptive were ten-times more likely to have to undergo reoperation than those who had their tubes tied. Source

 

 

If you received the Essure birth control device and suffered serious side effects and complications, you may be eligible for compensation.

 

 

IF YOU HAVE BEEN INJURED FROM THE

YOU MAY BE ELIGIBLE FOR COMPENSATION

More than 26,000 adverse event reports have been filed with the FDA over the severe side effects and devastating complications of the Essure device.

CALL FOR FREE CONSULTATION

CALL FOR FREE CONSULTATION

832-690-4053

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Breaking News: Sales of Essure birth control implant halted by Bayer

The U.S. Food and Drug Administration was notified by Bayer that the Essure permanent birth control device will no longer be sold or distributed after December 31, 2018.

  FDA Notice: July 20th 2018  

The U.S. Food and Drug Administration was notified by Bayer that the Essure permanent birth control device will no longer be sold or distributed after December 31, 2018.

 FDA Notice July 20th 2018 

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