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Essure Market Removal Remains Elusive

Essure remains on the market in the US but the word is getting out to be cautious of the controversial birth control device

Thursday, June 21, 2018 - The Essure Birth Control device has been implanted in hundreds of thousands of women around the world. There are many reasons for its popularity as opposed to other methods of birth control such as tubal ligation or hysterectomy. Essure can be administered in the comfort and convenience of a doctor's office and a woman can be up and around in a few hours. Essure is a metal coil that resembles the spring on a ballpoint pen. The device is inserted into the vagina and attaches itself to the Fallopian tubes. Each Essure, one per side, is intended to cause irritation and trigger the body's natural reaction causing scar tissue to develop around the device. After a few months, the device blocks a man's sperm from reaching a woman's eggs causing contraception. Essure is 99.8% effective.

Soon after women started using Essure, problems started to develop. One of the more consequential problems is that the Essure device can break away from the Fallopian tube wall and migrate to other parts of a woman's reproductive system and perforate them. Essure removal is tricky and complicated if a woman can find a doctor even willing to attempt an Essure removal procedure.

Thiry five thousand women, one congressman, and a world-famous investigator, Erin Brockovich, have drawn considerable attention to the fact that Essure Birth Control Device causes severe physical and psychological adverse symptoms to the women that carry the birth control device inside of them. The women's complaints to have the device taken off of the US market until further studies can be conducted have alerted the FDA to force Essure doctors and their potential Essure patients to complete and sign a comprehensive questionnaire certifying that the patient understands that the device is permanent and that its removal could entail permanent and irreversible sterilization.

In addition to the detailed questionnaire required of Essure patients in the US, a clinical study is underway in France to test women's condition after having had their Essure birth control device removed. The study will choose 70 women that currently allege to be experiencing certain symptoms they attribute to Essure and to see if three months after removing Essure, the symptoms have subsided and they feel better. Women that qualify for the study will be asked to certify that they are currently experiencing pain, bleeding, allergies fatigue, or articular pain, caused by Essure. The women will undergo a 3D ultrasound to make sure Essure is where it belongs, attached to the inner walls of the Fallopian tubes and has not migrated to another part of the body. The primary study seeks simply to ask if a woman feels better after having Essure removed and if the specific symptoms she complained about have subsided. Three months after surgery to remove Essure, women will be asked if they are feeling less depressed and if their Essure anxiety has gone away. The women will be given skin tests to determine if an allergic reaction to the metals in Essure such as Nickel remains. Lastly, women will be given tests to determine if an Essure remains in the body post removal.

Essure birth control lawsuits are being filed by women who have experienced a wide range of problems, including anxiety and depression.

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Onder Law is a St. Louis personal injury law firm handling serious injury and death claims across the country. Its mission is the pursuit of justice, no matter how complex the case or strenuous the effort. The Onder Law Firm has represented clients throughout the United States in pharmaceutical and medical device litigation such as Pradaxa, Lexapro and Yasmin/Yaz, where the firm's attorneys held significant leadership roles in the litigation, as well as Actos, DePuy, Risperdal and others, and other law firms throughout the nation often seek its experience and expertise on complex litigation.