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.
Allergan Biocell Lawsuit Claims Company Abandoned Implant Recipients After Cancer Recall September 3, 2020 Irvin Jackson Add Your CommentsAccording to allegations raised in a recently-filed lawsuit, Allergan has abandoned women who have their recalled breast implants, which may increase their risk of developing a rare form of cancer known as breast implant-associated anaplastic large cell lymphoma (BIA-ALCL).In a complaint (PDF) filed in the U.S. District Court for the District of New Jersey on August 19, Sachiko Jungbluth indicates that Allergan should be forced to pay for the removal and replacement of breast implants with the recalled Biocell macrotextured design linked to the problems.Jungbluth, of Houston, Texas, indicates she received bilateral Allergan Biocell Natrelle Silicone-Filled Textured breast implants in November 2014. However, five years later in July 2019, Allergan announced a Biocell breast implant recall, after they were linked to an increased risk of BIA-ALCL.Learn More AboutBreast Implant LawsuitsWomen may face a risk of Anaplastic Large Cell Lymphoma (ALCL) from certain breast implants.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONLearn More AboutBreast Implant LawsuitsWomen may face a risk of Anaplastic Large Cell Lymphoma (ALCL) from certain breast implants.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONโAs a direct and proximate result of her Biocell implants, Plaintiff is at an increased risk of developing BIA-ALCL,โ the lawsuit notes. โHad Plaintiff been informed that Biocell would expose her to an increased risk of BIA-ALCL, she would have never had the Biocell implant installed.โJungbluth indicates Allergan has refused to pay for the removal and replacement of recalled breast implants, indicating that herself and other women with the breast implants face a continuing risk from the design, even if they have not been diagnosed with BIA-ALCL.Allergan has faced growing litigation since the recall, including a number of breast implant lymphoma lawsuits brought by women diagnosed with BIA-ALCL, as well as individual actions for women who required removal of the breast implants and class action claims for women who need future medical monitoring.The complaint will be consolidated with other similar lawsuits filed throughout the federal court system, which are centralized for pretrial proceedings before U.S. District Judge Brian R. Martinotti in the District of New Jersey, as part of a federal MDL, or multidistrict litigation.Given common questions of fact and law raised throughout the litigation, it is expected that Judge Martinotti will select a small group of representative claims for early trial dates to help the parties gauge how juries may respond to certain evidence and testimony that is likely to be repeated throughout the litigation. However, as more women discover that they have BIA-ALCL or decide to have the breast implants removed, the size and scope of the litigation is expected to continue to expand over the coming months. 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: Allergan, Allergan Biocell, Anaplastic Large Cell Lymphoma, Breast Implant, Breast Implant Cancer, Breast Implant Lymphoma, CancerMore Breast Implant Lawsuit Stories Breast Implant Lymphoma Risk May Extend Beyond ALCL, Researchers Warn August 22, 2025 Breast Implants After Mastectomy May Increase Risk of ALCL for Some Women: Study June 30, 2025 Study Finds Rising Breast Cancer Rates Among Young Women October 14, 2024 0 Comments 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 Depo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims (Posted: 2 days ago)A Depo-Provera meningioma lawsuit indicates that a woman suffered permanent and debilitating injuries after needing to have a brain tumor surgically removed.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Caused Meningioma 29 Years After First Birth Control Shots: Lawsuit (05/22/2026)Depo-Provera Lawsuit Filings Exceed 6,000, As Court Prepares for First Test Trials (05/18/2026)Intracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (05/12/2026) Dupixent Injection Lawsuit Alleges Manufacturer Failed to Warn About T-Cell Lymphoma Cancer Side Effects (Posted: 3 days ago)Regeneron and Sanofi-Aventis face a Dupixent injection lawsuit from a Louisiana woman who says the companies knew about the drug’s risks but downplayed them to doctors and patients.MORE ABOUT: DUPIXENT LAWSUITDupixent Cancer Lawsuit Claims Eczema Drug Caused Womanโs CTCL Diagnosis (05/28/2026)Link Between Dupixent and Cancer Withheld From Doctors and Users, Lawsuit Alleges (05/11/2026)Lawsuit Indicates Dupixent Lymphoma Diagnosis Resulted in Multiple Rounds of Chemotherapy (05/01/2026) Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (Posted: 4 days ago)A Nevada woman has filed a lawsuit alleging defects in AngioDynamicsโ port catheters caused her Xcela device to trigger a thrombosis in her right internal jugular vein.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITSmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body (05/15/2026)18 AngioDynamics Port Catheter Lawsuits Will Be Selected for Bellwether Discovery in August 2026 (05/05/2026)AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism (04/30/2026)
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