Scope Infection Lawsuit Patients across the United States have filed medical scope infection lawsuits after contaminated endoscopes and duodenoscopes allegedly transmitted dangerous bacterial infections during procedures such as ERCP, colonoscopy, and other endoscopic treatments.
Spinal Cord Stimulator Lawsuit Spinal cord stimulator lawsuits allege that implanted pain devices malfunctioned, migrated, or caused nerve damage, often forcing patients to undergo revision or removal surgery.
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.
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.
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
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.
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.
Breast Mesh Lawsuit Lawyers are investigating breast mesh lawsuits for women who suffered infections, pain, or implant failure from internal bra implants used in breast reconstruction surgery.
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.
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.
ParaGard IUD Lawsuit Filed Over Risk Birth Control Implant May Break During Removal Surgery June 3, 2020 Irvin Jackson Add Your CommentsAn Illinois woman has filed a product liability lawsuit over problems with the ParaGard IUD, indicating that the intrauterine birth control device is defective and prone to break at the arms during explant surgery, resulting in a risk of serious injuries.The complaint (PDF) was filed by Beth Parker in the U.S. District Court for the Southern District of Illinois on May 28, naming Teva Pharmaceuticals, The Cooper Companies, Inc., and Coopersurgical, Inc. as defendants.ParaGard is a copper IUD birth control implant, involving a T-shaped plastic frame that is wrapped with copper wire coils, which are designed to produce an inflammatory reaction in the uterus that is toxic to sperm and prevents pregnancy. The birth control device is supposed to remain in place for up to 10 years, but is intended to be removable and allow women to conceive after it is explanted.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 COMPENSATIONAccording to allegations raised in the Paragard IUD lawsuit filed by Parker, when she went to have the device removed in May 2018, about ten years after it was implanted, it broke and left one of the arms behind inside her body.Parker indicates neither she, nor her doctor, were warned about the risk of that the Paragard IUD may fracture or break during removal, leaving her with painful and potentially permanent injury.โPrior to Plaintiff being implanted with the ParaGard IUD, Defendants knew and should have known that the drug was defective and unreasonably dangerous,โ the lawsuit states. โTeva and Cooper Defendants knew or should have known that ParaGard can and does cause serious harm to individuals who use it, due to the risk of the ParaGardโs arm breaking upon removal.โThe lawsuit presents claims of negligence, design defect, manufacturing defect, failure to warn, common law fraud, negligent misrepresentation, breach of warranty, violation of consumer protection laws, and gross negligence. She is seeking both compensatory and punitive damages.Parker’s claim isย one of several Paragard IUD lawsuits filed in recent years, involving similar allegations of problems during removal surgery. 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: Birth Control Device, IUD, Paragard, Teva PharmaceuticalsMore Paragard IUD Lawsuit Stories Lawsuit Over Paragard IUD Removal Risks Results in Defense Verdict February 5, 2026 Paragard MDL Judge Indicates First Bellwether Trial Will Move Forward as Scheduled January 14, 2026 First Paragard IUD Lawsuit Set for Jury Trial To Begin Jan. 20, 2026 December 29, 2025 0 Comments FacebookThis 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 Abbott Eterna Lawsuit Alleges Spinal Cord Stimulator Malfunction Resulted in Worsening Pain (Posted: today)According to a lawsuit brought against the manufacturer and the FDA, an Abbott Eterna spinal cord stimulator has caused pain, shocks and complications instead of the relief promised.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Stimulator Lawsuit Alleges SCS Lead Failure Caused Nerve Damage (05/06/2026)Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (04/29/2026)JPML Sets Hearing Over Spinal Cord Stimulator Lawsuit Consolidation for May 28 (04/24/2026) Intracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (Posted: yesterday)A Depo-Provera intracranial meningioma lawsuit claims Pfizer developed and sold a defective birth control injection that puts women at a five times increased risk of brain tumors.MORE ABOUT: DEPO-PROVERA LAWSUITLawsuit Blames Depo Shot for Brain Tumors, Intense Headaches (04/28/2026)Depo-Provera Meningioma Warning Update Should Be Added to Birth Control Shot: Lawsuit (04/22/2026)Hearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (04/15/2026) Link Between Dupixent and Cancer Withheld From Doctors and Users, Lawsuit Alleges (Posted: 2 days ago)A lawsuit alleges an Illinois woman developed CTCL after using Dupixent, raising concerns the manufacturer may have withheld concerns that the drug could contribute to cancer.MORE ABOUT: DUPIXENT LAWSUITLawsuit Indicates Dupixent Lymphoma Diagnosis Resulted in Multiple Rounds of Chemotherapy (05/01/2026)Judges Will Consider MDL for Dupixent Cancer Lawsuits Late Next Month (04/21/2026)Dupixent Injections Caused Peripheral T-Cell Lymphoma (PTCL) Diagnosis: Lawsuit (04/06/2026)
Abbott Eterna Lawsuit Alleges Spinal Cord Stimulator Malfunction Resulted in Worsening Pain (Posted: today)According to a lawsuit brought against the manufacturer and the FDA, an Abbott Eterna spinal cord stimulator has caused pain, shocks and complications instead of the relief promised.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Stimulator Lawsuit Alleges SCS Lead Failure Caused Nerve Damage (05/06/2026)Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (04/29/2026)JPML Sets Hearing Over Spinal Cord Stimulator Lawsuit Consolidation for May 28 (04/24/2026)
Intracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (Posted: yesterday)A Depo-Provera intracranial meningioma lawsuit claims Pfizer developed and sold a defective birth control injection that puts women at a five times increased risk of brain tumors.MORE ABOUT: DEPO-PROVERA LAWSUITLawsuit Blames Depo Shot for Brain Tumors, Intense Headaches (04/28/2026)Depo-Provera Meningioma Warning Update Should Be Added to Birth Control Shot: Lawsuit (04/22/2026)Hearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (04/15/2026)
Link Between Dupixent and Cancer Withheld From Doctors and Users, Lawsuit Alleges (Posted: 2 days ago)A lawsuit alleges an Illinois woman developed CTCL after using Dupixent, raising concerns the manufacturer may have withheld concerns that the drug could contribute to cancer.MORE ABOUT: DUPIXENT LAWSUITLawsuit Indicates Dupixent Lymphoma Diagnosis Resulted in Multiple Rounds of Chemotherapy (05/01/2026)Judges Will Consider MDL for Dupixent Cancer Lawsuits Late Next Month (04/21/2026)Dupixent Injections Caused Peripheral T-Cell Lymphoma (PTCL) Diagnosis: Lawsuit (04/06/2026)