Recalled Medical Devices Fast-Tracked Through FDA Approval Process Were Often Based on Flawed, Older Designs: Study
Sports Betting Addiction Lawsuit Sports betting addiction lawsuits are being investigated for college students and young adults who developed gambling problems after using apps like FanDuel and DraftKings, alleging that the platforms failed to warn about the addictive nature of their features and marketing practices.
Nitrous Oxide Lawsuit Individuals who suffered harm, or families who lost a loved one after using nitrous oxide products may be eligible for financial compensation through a nitrous oxide lawsuit.
Hair Relaxer Lawsuit Regular exposure to chemicals in hair relaxer may cause uterine cancer, ovarian cancer and other injuries. Women diagnosed with cancer may be eligible for settlement benefits.
Depo-Provera Lawsuit Depo-Provera lawsuits are being investigated for women who developed meningioma brain tumors after receiving Depo-Provera birth control shots, claiming that Pfizer failed to adequately disclose side effects.
Ozempic Lawsuit Lawyers are pursuing Ozempic lawsuits, Wegovy lawsuits and Mounjaro lawsuits over gastroparesis or stomach paralysis, which can leave users with long-term gastrointestinal side effects
Suboxone Tooth Decay Lawsuit Lawsuits are being pursued by users of Suboxone who experienced tooth loss, broken teeth or required dental extractions. Settlement benefits may be available.
Change Healthcare Lawsuit Lawyers are reviewing Change Healthcare class action lawsuits for individuals who had their personal information stolen due to the data breach.
Bard PowerPort Lawsuit Serious and life-threatening injuries have been linked to problems with Bard PowerPort. Lawsuits are now being pursued by individuals who suffered injuries from the implantable port catheter fracturing or migrating.
AngioDynamics Port Catheter Lawsuit Serious and life-threatening injuries have been linked to problems with Bard PowerPort. Lawsuits are now being pursued by individuals who suffered injuries from the implantable port catheter fracturing or migrating.
Processed Food Lawsuit Lawsuits are being pursued against the food industry over their manufacturing and advertising of ultra-processed foods, which have caused a generation of children to face an increased risk of developing childhood diabetes and other chronic illnesses.
Vaginal Mesh Surgery Complication Risk High, Despite Effectiveness: Study May 16, 2011 Staff Writers Add Your Comments The use of vaginal mesh to treat pelvic organ prolapse is effective, but does carry a high risk of serious complications, such as bladder perforation and pelvic hemorrhage, according to the findings of a new study. In a study published last week in the New England Journal of Medicine, European researchers found that vaginal mesh surgery brought better results for treating pelvic organ prolapse than stitching the connective tissue in the vaginal wall back together, but carried risks of surgical complications and other problems after surgery, including pain during sex and new urinary incontinence. A pelvic organ prolapse occurs when organs such as the bladder, uterus, bowel or rectum drop and push against the wall of the vagina. This happens when the muscles holding the pelvic organ in place become weak or stretched, often due to childbirth or surgery. The vaginal mesh is used to support the muscle. Learn More About Vaginal Mesh / Bladder Sling Lawsuits Complications from transvaginal mesh may cause severe injuries. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Learn More About Vaginal Mesh / Bladder Sling Lawsuits Complications from transvaginal mesh may cause severe injuries. Learn More SEE IF YOU QUALIFY FOR COMPENSATION For the study, researchers looked at 389 women who were treated for pelvic organ prolapse. Vaginal mesh was implanted in 200 of them, while the remaining 189 were treated with colporrhaphy, the traditional stitching of the vaginal wall. Researchers found that after one year, about 61% of the women who were treated with a vaginal mesh were absent of the symptoms of prolapse, compared to only 34.5% of the women who received colporrhaphy. However, there were a number of potentially serious problems with the vaginal mesh reported, including reports of inter-operative hemorrhaging. About 3.5% of women who received vaginal mesh suffered a bladder perforation during the surgery, compared to only 0.5% of the women who received colporrhaphy. The rate of urinary incontinence was nearly doubled, with 12.3% for women who received a mesh experiencing the problem, compared with only 6.3% for a colporrhaphy. Researchers also found that 3.2% of the women who received the mesh required follow-up surgery to correct exposure problems. The findings come just months after some doctors publicly expressed concern about the risks associated with vaginal mesh surgery. In a Letter to the Editor published in the American Journal of Obstetrics & Gynecology in November, one doctor suggested that there is a lack of sound scientific information on vaginal mesh health risks. Dr. Anne M. Weber, of Pennsylvania, told the journal that a lack of information made it impossible for patients to give informed consent and suggested all vaginal mesh surgery be considered experimental. Problems with vaginal mesh manufactured by several different companies have led to product liability lawsuits filed by women who have experienced infections, erosion of the vaginal mesh and other painful complications. Last year, settlements were reached in a number of Mentor ObTape vaginal mesh lawsuits filed by women who alleged that the complication rate associated with that product could be as high as 17% to 18%. The Mentor ObTape was removed from the market in 2006, only three years after it was introduced. A growing number of Bard Avaulta vaginal mesh lawsuits have also been filed by women who have experienced problems. All of the complaints involve similar allegations that C.R. Bard’s Avaulta Anterior and Posterior BioSynthetic Support System, which was introduced in 2007, was negligently designed and that the company failed to warn patients of possible complications that can result in severe pain and disfigurement. In October, all the federal Bard Avaulta litigation was consolidated as part of an MDL for pretrial proceedings in the U.S. District Court for the Southern District of West Virginia. At the time, there were at least 36 different Bard Avaulta lawsuits located in federal courts across the country. However, Bard Avaulta mesh lawyers are continuing to review and file potential lawsuits, and the number of complaints is expected to grow in the coming months. Tags: Bard, Bard Avaulta, Bard Avaulta Mesh, Informed Consent, Mentor, New England Journal of Medicine, ObTape, Surgical Mesh, Vaginal Mesh Image Credit: | More Vaginal Mesh Lawsuit Stories Study Finds Some Transvaginal Mesh Degrades Within 2 Months After It Is Implanted October 29, 2024 Supreme Court Rejects J&J Bid to Overturn $302M Vaginal Mesh Lawsuit Award February 23, 2023 Recalled Medical Devices Fast-Tracked Through FDA Approval Process Were Often Based on Flawed, Older Designs: Study January 16, 2023 0 Comments 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 No Post Comment I authorize the above comments be posted on this page Weekly Digest Opt-In Yes, send me a weekly email with the latest lawsuits, recalls and warnings. 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Recalled Medical Devices Fast-Tracked Through FDA Approval Process Were Often Based on Flawed, Older Designs: Study January 16, 2023
MDL Judge Orders Paraquat Lawsuit Settlement Update By June 11, 2025 (Posted: today) A federal judge has agreed to stay all case-specific discovery deadlines in Paraquat lawsuits, while the parties work to hammer out a settlement agreement to resolve thousands of claims. MORE ABOUT: PARAQUAT PARKINSON’S DISEASE LAWSUITSParaquat Settlement Reached for Parkinson’s Disease Lawsuits Filed in MDL (04/16/2025)Appeals Court Urged To Reinstate Paraquat Lawsuits Previously Set for Bellwether Trials (02/14/2025)Paraquat Lawsuits Over Parkinson’s Disease Risk Set for Trial in October 2025, April 2026 (01/29/2025)
Court Outlines Requirements for Depo-Provera Lawsuit Proof of Use, Type of Meningioma Tumor (Posted: yesterday) As new Depo-Provera lawsuits continue to be filed, the judge presiding over the litigation has established key criteria for establishing proof of Depo-Provera use and medical documentation confirming a meningioma diagnosis. MORE ABOUT: DEPO-PROVERA LAWSUITDepo Shot Lawsuit Filed Over Serious Brain Tumor Injuries (05/07/2025)Lawsuit Alleges Depo-Provera Migraines, Headaches Led to Meningioma Brain Tumor Diagnosis (05/01/2025)Depo-Provera Hearing Loss Lawsuit Filed Over Brain Tumor Side Effects (04/22/2025)
BioZorb Implant Lawsuit Alleges Tissue Marker Caused Swelling, Fluid Buildup and Chronic Pain (Posted: 2 days ago) A Massachusetts woman’s injuries from a failed tissue marker that was recently recalled led to the need for physical therapy, according to a BioZorb implant lawsuit. MORE ABOUT: BIOZORB LAWSUITFour Women File BioZorb Lawsuit Over Breast Tissue Marker Failures and Injuries (05/05/2025)Lawsuit Claims BioZorb Marker Caused Chronic Pain, Multiple Surgeries After Lumpectomy (04/14/2025)Four BioZorb Breast Tissue Marker Lawsuits Selected for Bellwether Trials (04/02/2025)