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The FDA May Have Ignored Thousands Of Essure Complaints

Essure doctors failed to disclose Essure's shortcomings and never reported patient complaints to the FDA

Thursday, June 27, 2019 - The US Food and Drug Administration is under as much pressure today as Bayer Inc., the current manufacturer, and seller of the Essure birth control device. Nearly 50,000 women have written about their horrendous and life-altering experiences that occurred after having Essure inserted into their Fallopian tubes. The FDA admits that they have received around 25,000 complaints about Essure but IT experts think that the number could be exponentially greater.

There are a number of basic problems plaguing Essure users. The first is that the device often does not become firmly embedded on the inner wall of the Fallopian tubes as intended and instead migrates into the uterus where contraction to expel the foreign object only sink Essure's sharp edges deeper and deeper into the organ's tissues, lacerating and puncturing it, and causing constant and extreme pain and non-stop heavy vaginal and internal bleeding. The only solution for women is to have a radical hysterectomy to remove their entire reproductive system in order to get at and remove the metal coil. This Essure defect alone should have been enough for the FDA to recall the device and stop it from being sold. Essure problems lawyers are helping families and individuals in the United States and offer a free consultation before filing a claim.

Another obstacle that Essure women face is their gynecologist's unwillingness to even admit that Essure could be causing their pain and bleeding without even performing an examination and telling most Essure women that complain that "they are crazy or that the pain is just in their head." When a woman has been rendered bed-ridden from Essure the last thing they want to hear is that their doctor can do nothing. In reality, few if any doctors that implant their patients with Essure have the training necessary to remove them. When an untrained surgeon tries to yank Essure coils from the reproductive organ tissues where it has become encased in scar tissue, the device often breaks and only a fraction is removed.

Essure was originally made and marketed by Conceptus, Incorporated which Bayer acquired June 5, 2013. The FDA originally approved Essure on November 02, 2002. The FDA's description of the device at the time was "a permanently implanted birth control device for women." As a Class III medical device, Essure was subject to the most stringent testing using the pre-market approval process (PMA). In addition, the FDA required Essure to undergo two post-approval studies to follow up on the original premarket clinical trials and gather data on how Essure was performing. According to the FDA, the post-market study examined: "how well Essure prevented pregnancy, the safety of the procedure used to place Essure and, the safety of Essure once implanted, including patient comfort." Since then, the ongoing regulatory approval of Essure has forced the labeling of the device to undergo so many changes to its safety profile that one is left wondering what testing the FDA performed on Essure in the first place and Essure women are left with more questions than answers. How could the FDA miss the tens of thousands of complaints that were registered by Essure victims over the last decade? Why were Essure doctors never required to report complaints by their patients to the FDA? Why are so many Essure doctors on the Bayer payroll receiving backdoor commissions for selling Essure and labeling the payments as educational and speaking fees?

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OnderLaw, LLC 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. OnderLaw 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.