Study of Recalled Essure Implant Continues to Lose Participants, But FDA Reports Measures to Fix Data are Working
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Essure Problems Highlighted at Patient Protest Outside Conference November 13, 2013 Irvin Jackson Add Your CommentsA group of women gathered last weekend outside of a conference on gynecological surgery, in an effort to bring attention to thousands of reports involving complications and serious injuries linked to Essure birth control implant. ย About half a dozen protesters spent the weekend outside of the 42nd Global Congress of Minimally Invasive Gynecology at the National Harbor, just outside of Washington, D.C. The protesters held up signs outlining the Essure birth control problems they had allegedly suffered.The event is held by the AAGL, which once stood for the American Association of Gynecologic Laparoscopists, but is officially now just the AAGL anagram due to its international reach. The Essure protesters were allowed a private meeting with the AAGL Executive Committee.Learn More AboutParagard LawsuitsWomen have reported problems where Paragard IUD fractured or broken during removal, resulting in serious injury.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONLearn More AboutParagard LawsuitsWomen have reported problems where Paragard IUD fractured or broken during removal, resulting in serious injury.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONAs a result of that meeting, the committee reportedly promised to send out memos to the thousands of members of their organization that will inform the members about the potential risk of Essure complications.Essure birth control is a transcervical sterilization procedure, which is marketed as a less expensive, easier and safer alternative to tubal ligation surgery. Approved by the FDA in 2002, Essure was originally designed and manufactured by Conceptus, before being acquired by the pharmaceutical giant Bayer.More than 750,000 women have undergone Essure birth control surgery, according to prior data released by Conceptus, and hundreds of adverse event reports have been filed with the FDA over the past decade involving problems that could be linked to side effects of Essure implants.The birth control implant is offered as an outpatient procedure by many medical facilities. During the surgery, a doctor inserts bendable coils into the fallopian tubes, passing through the vagina, cervix and uterus. The process thus causes scar tissue to form around the coils over several months, which blocks the tubes, preventing insemination.Problems reportedly linked to Essure include puncturing of the fallopian tubes and uterus, allergic reactions, reports of the implants breaking inside women’s bodies and other side effects. The FDA reports alone detail nearly 100 women who have had to undergo hysterectomies due to Essure side effects.Bayer, which bought the original company that made the Essure implant and now markets the device worldwide, has downplayed the complaints, saying that there are relatively few cases out of the Essure implants used worldwide. Written by: Irvin JacksonSenior Legal Journalist & Contributing EditorIrvin Jackson is a senior investigative reporter at AboutLawsuits.com with more than 30 years of experience covering mass tort litigation, environmental policy, and consumer safety. He previously served as Associate Editor at Inside the EPA and contributes original reporting on product liability lawsuits, regulatory failures, and nationwide litigation trends. Tags: Bayer, Birth Control, Essure, Washington Image Credit: |More Essure Lawsuit Stories Study of Recalled Essure Implant Continues to Lose Participants, But FDA Reports Measures to Fix Data are Working November 1, 2023 Progress of Essure Birth Control Implant Post-Marketing Study “Inadequate,” FDA Warns Bayer October 11, 2022 85% of Bayer Essure Adverse Event Reports Submitted Last Year Linked to Device Removal: FDA March 16, 2022 1 Comments Brandi January 10, 2016 I’ve made comments twice already and no one is listening I’ve had this procedure done cause my doctor recommended it and I have had major problems in my past health history including SVT,intestinal surgery,wilms tumor stage three and I’m seriously concerned about this since it has been causing so much pain and I haven’t stopped bleeding since the procedure I’m just getting more depressed about cause my doctor is not listening to my issues and I think it’s time to make a step towards this lawsuits can u help me……Brandi URLThis field is for validation purposes and should be left unchanged.Share Your CommentsFirst Name*Last NameEmail* Shared Comments*This field is hidden when viewing the formI authorize the above comments be posted on this page Yes NoPost Comment I authorize the above comments be posted on this pageWeekly Digest Opt-In Yes, send me a weekly email with the latest lawsuits, recalls and warnings.Want your comments reviewed by a lawyer?To have an attorney review your comments and contact you about a potential case, provide your contact information below. This will not be published.Contact Phone #Alt Phone #Private CommentsNOTE: Providing information for review by an attorney does not form an attorney-client relationship.CAPTCHAGA SourceGA CampaignGA MediumGA ContentGA TermΔ MORE TOP STORIES Suboxone Dry Mouth Lawsuit Claims Dental Problems Could Have Been Avoided With Sublocade Shot (Posted: 4 days ago)Five plaintiffs say they all suffered dental problems due to the side effects of Suboxone, which could have been avoided with adequate warnings.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (06/11/2026)Suboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (05/20/2026)Lawsuit Alleges Suboxone Dental Damage Warnings Were Issued Too Late (05/07/2026) Lawsuit Claims Dupixent Cancer Diagnosis Occurred After Only 8 Months of Use (Posted: 5 days ago)The makers of Dupixent face a CTCL lawsuit by a man who says he developed the rare form of cancer less than a year after beginning treatment with the eczema drug.MORE ABOUT: DUPIXENT LAWSUITRezurock Lawsuit Claims GVHD Medication Caused Debilitating Skin Condition, Prurigo Nodularis (06/12/2026)Dupixent Injection Lawsuits Consolidated in MDL Over CTCL Diagnoses (06/09/2026)Dupixent Injection Lawsuit Alleges Manufacturer Failed to Warn About T-Cell Lymphoma Cancer Side Effects (06/04/2026) Abbott Spinal Cord Stimulator Battery Problems Led to Repeat Surgeries, Lawsuit Claims (Posted: 6 days ago)Four plaintiffs allege Abbott spinal cord stimulator battery problems, painful malfunctions and other device failures caused worsening symptoms and repeat surgeries after the company made hundreds of changes to its implant systems.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (06/12/2026)Boston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026)Lawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (06/02/2026)
Study of Recalled Essure Implant Continues to Lose Participants, But FDA Reports Measures to Fix Data are Working November 1, 2023
Progress of Essure Birth Control Implant Post-Marketing Study “Inadequate,” FDA Warns Bayer October 11, 2022
85% of Bayer Essure Adverse Event Reports Submitted Last Year Linked to Device Removal: FDA March 16, 2022
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