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Essure Victims Lobby the FDA to Take Essure Off The Market

The FDA has responded to Essure womens concerns by producing a questionnaire that, along with their doctors, they must review and sign

Wednesday, May 16, 2018 - Thousands of women have filed reports with the Food and Drug Administration that Essure Birth Control Device caused their constant and debilitating pain. Many of these same women have connected with each other in the Facebook group entitled, Essure Problems. In Essure Problems, women from around the country are free to post about the endless array of adverse side effects Essure causes and that they were not made aware of prior to having Essure implanted. Most if not all of the Essure women had never even heard of Essure until they visited their gynecologist looking for a method of sterilization.

Women, frustrated with the FDA's unwillingness to take Essure off of the market pending further testing, have further organized and have met with officials including the FDA commissioner to present their case for taking Essure off the market.

As a result of the Essure women's efforts as well as the involvement of a US congressman, changes have been made to make sure women know Essure's risks before they choose a method of birth control in order to make a more informed decision. Essure doctors must pass specific Essure training and doctors and patients must review a lengthy questionnaire that details the side effects and the likelihood they will occur. The patient is required to sign the document if they choose to undergo the procedure.

Women who are contemplating using Essure birth control must know that the device that is meant to remain in place attached to the inside of the Fallopian tube can detach and travel to the uterus and puncture it. This is one of the more common complaints against using Essure. A second complaint is that if a woman wishes to have the Essure device removed, doctors capable and willing to do the procedure are few and far between. Gynecologists are not specifically trained to remove Essure and even if you can find a specialist you may be forced to travel many miles at your expense to have it done. Such a procedure could involve having all or part of a woman's reproductive system removed as well. Other than having a hysterectomy, Essure patients may not be able to have the device only removed. Even if Essure is attached where it belongs to the inside wall of the Fallopian tube, it may be so encased in scar tissue that its removal alone will be impossible and the patient will need a partial hysterectomy.

The upshot of the FDA requiring Essure women to sign and certify they have read and understood the side effects may have unintended results. Signing the questionnaire may be tantamount to signing away your right to file a claim against the company if one of the side effects does in fact occur. Before signing anything, women should visit the Facebook group, Essure Problems and talk with women who have had their lives adversely affected by the Essure birth control device they thought was safe. There have been thousands of Essure complications lawsuits filed with no end in sight.

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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.