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Stricter FDA Restriction Being Ignored by Physicians

Essure doctors are failing to comply with the FDA order and implanting unsuspecting women with the defective Essure birth control device

Monday, July 2, 2018 - In April of 2018, the US Food and Drug Administration (FDA) ordered restrictions placed upon doctors that recommend their patients use the Essure birth control device. Doctors are required to sit down with a patient and go over a questionnaire with them that is designed to alert them to the risks of permanent sterilization from having Essure implanted. This questionnaire must be signed by the doctor and the patient and submitted to the FDA before permission is given to implant Essure. The FDA's goal is to make sure that potential Essure patients have all of the information they need to make an informed decision.

Such a move to restrict Essure is in response to the concerns of over 5000 women that have filed adverse event reports with the FDA claiming an almost limitless number of life-altering and unforeseen side effects after having, at the behest of their doctor, the device implanted. Women posting on social media have reported over 20000 instances of adverse symptoms including but not limited to heavy bleeding, total and debilitating body aches, auto-immune reactions, body rashes, severe pain in their reproductive organs, nausea, headaches, extreme fatigue and many more symptoms.

In short, Essure looks like the spring coil in a retractable ballpoint pen and the device is inserted into the vagina, past the cervix, and placed on the inner walls of the Fallopian tubes, one in each side. Over the next three months, scar tissue develops to block the pathway of a man's sperm preventing fertilization.

According to Cnn.com, the problem with the new restrictions placed on Essure is that doctors are not complying with the FDA's requirements. Facebook group Essure Problems, a 36,000 member strong community of women who suffer from the adverse side effects of Essure, report that most women, over 90% are not getting the Essure warnings and required questionnaire and being implanted with Essure nonetheless.

Women that are experiencing the adverse side effects of Essure normally look to alleviate their suffering by having the device removed. Such removal, however, is fraught with complications. One thing that most complications have in common, however, is the fact that Essure removal almost always requires a partial or complete hysterectomy, the same dangerous and invasive surgery that an Essure patient was hoping to avoid. In addition, Essure frequently disintegrates into several pieces that are difficult to find within the body so that when some of Essure is removed, parts of it can be left behind causing the symptoms to continue. When Essure can actually be located intact it often has migrated to another part of a woman's reproductive system and has caused damage requiring the organ's removal along with the Essure device.

Thousands of Essure women have consulted Essure attorneys and have filed a claim against Essure maker Bayer claiming the company has brought a faulty medical device to market without sufficient testing and failed to warn women of the potential negative consequences of the birth control device.

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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.