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.
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.
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.
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.
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.
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.
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.
Dupixent Lawsuit Dupixent lawsuits are being investigated for patients who developed rare blood cancers such as cutaneous T-cell lymphoma (CTCL) after receiving injections, alleging that Sanofi and Regeneron failed to warn about the potential risks of immune suppression and delayed cancer diagnosis.
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.
DePuy Prodigy Stem Lawsuit Alleges Hip Implant Is Defective February 15, 2016 Irvin Jackson Add Your Comments Johnson & Johnson faces a product liability lawsuit over its DePuy Prodigy femoral stem, indicating that the hip implant was defectively designed and caused a woman to experience complications that required the device to be surgically removed. The complaint (PDF) was filed by Joan Conboy Miller in the U.S. District Court for the Eastern District of Northern Carolina on February 12, naming Johnson & Johnson and its DePuy subsidiary as defendants. Miller indicates that she underwent left-side total hip replacement surgery in October 2006, at which time she received a DePuy Prodigy Stem, lined to a DePuy Pinnacle Acetabular Cup and other components. As a result of problems with the DePuy Prodigy stem, Miller indicates that she ended up undergoing revision surgery in February 2013, although the device was expected to last much longer. Stay Up-to-Date About hip replacement lawsuits AboutLawsuits.com sends a weekly digest email with information about recalls, lawsuits and warnings that may impact your family, which will include any new hip replacement lawsuit updates or developments. "*" indicates required fields Email* SIGN ME UP Δ Learn More Stay Up-to-Date About Hip Replacement Lawsuits AboutLawsuits.com sends a weekly digest email with information about recalls, lawsuits and warnings that may impact your family, which will include any new hip replacement lawsuit updates or developments. "*" indicates required fields Email* SIGN ME UP Δ Learn More The lawsuit indicates that the stem failed because it was not manufactured in accordance with Current Good Manufacturing Practice (CGMP) regulations. Miller also claims that the true DePuy Prodigy failure rates are higher than those the manufacturer has reported to the FDA. “DePuy received numerous reports of failures of Prodigy stems prior to the date of Plaintiff’s implant and revision similar to the failure alleged by Plaintiff,” the lawsuit states. “At the same time, there were and are safer alternative artificial hip products readily available in the marketplace from other manufacturers which do not have elevated failure rates.” The lawsuit presents claims against the medical device manufacturers for strict liability, negligence, breach of warranty, and failure to warn, seeking both compensatory and punitive damages. The manufacturer also faces thousands of DePuy Pinnacle hip lawsuits filed in courts throughout the United States, over problems linked to the metal-on-metal configuration of the artificial hip system. Plaintiffs allege that as the metal parts rub against each other, microscopic metal debris may be released into the body, increasing the risk of loosening and failure within a few years after the implant. Given the similar allegations raised in the cases, all DePuy Pinnacle lawsuits are centralized in the Northern District of Texas before U.S. District Judge Ed Kinkeade to reduce duplicative discovery into common issues in the cases, avoid conflicting rulings from different courts and to serve the convenience of the parties, witnesses and the courts. Written by: Irvin Jackson Senior Legal Journalist & Contributing Editor Irvin 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. Image Credit: test caption More Hip Replacements Lawsuit Stories Biomet Hip Lawsuit Filed Over Defective M2A Metal-on-Metal Implant December 26, 2024 Zimmer Biomet Lawsuit Filed Over RibFix Blu Implant Fracture September 25, 2024 Zimmer Biomet CPT Hip System Linked to Increased Risk of Thigh Bone Fractures, FDA Warns September 18, 2024 1 Comments Brian September 16, 2020 I have the DePuy Pinnacle stem and head , though my surgeon was smart enough to use the ceramic head and cup liner , I was diagnosed with a hairline fracture by bone s an with contrast about two years into the total hip replacement I had at age forty four . First discussing surgery , the surgeon who did the surgery decided to send me to pain management for the first time. I had numerous other ortho injuries due to a fall n the job , including a broken back and displaced L-5 vertebrae , multiple herniated discs in my cervical spine , shoulder and knee injuries. I feel very lucky to have survived the pain management , immediately put on a fentanyl patch and gabapentin , and others. After quitting pan management , another bone scan with contrast was done at about seven years post op , still a clear fracture running almost the length of what remained of my femur. I refused pain management , but about two and a half years later started with a much better doctor who uses much different medโs. My point is that I believe the crack was present from surgery until today , fifteen years in and I can definitely feel the stem failing , the hip is beginning to feel as it did before replacement. I lost five years living in a narcotic nightmare that I quit almost cold turkey and would never allow to happen again , unless I was terminal and n horrible pain. The last couple of years near the end I was having facet joint blocks in cervical and lumbar spine every three months , before that , single or series of three injections regularly . Iโve had two spinal injections in over five years with the current pain doctor. I feel it was all caused by and the femoral fracture was present from surgery. Like most , I immediately was pan free and felt like my life was given back after three and a half years of fighting with workers comp because I had an imbecile E/R doctor at hospital after the fall. Just wondering if anyone had similar problems or complains after receiving the DePuy stem with screen , non cemented , replacement stem ? NameThis 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 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. 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 Term Δ MORE TOP STORIES Lawyers To Nominate Hair Relaxer Cancer Cases for Early Bellwether Trials Next Week (Posted: today) Plaintiffs and defendants involved in hair relaxer cancer lawsuits are expected to turn in a list of 12 cases that the parties believe are fit to serve as bellwether trials. MORE ABOUT: HAIR RELAXER LAWSUITCourt Outlines Procedures When Women Die After Filing a Hair Relaxer Cancer Lawsuit (02/25/2026)Hair Extension Chemicals May Be More Harmful Than Previously Thought: Study (02/17/2026)MDL Judge Issues New Deadlines for Hair Relaxer Lawsuit Bellwether Trial Preparations (02/04/2026) Cartiva Implant Recall Lawsuits Move Forward, as Plaintiffs Seek Compensation for Big Toe Surgery Failures (Posted: yesterday) Cartiva implant lawsuits are moving forward in federal court as patients across the United States seek compensation for complications linked to the recalled big toe device. MORE ABOUT: CARTIVA IMPLANT LAWSUITCartiva Synthetic Cartilage Implant Lawsuits Centralized in Federal MDL (02/10/2026)Lawsuit Alleges Cartiva Implant Loosened, Degraded in Great Toe (02/05/2026)Big Toe Fusion Lawsuit Filed Over Failed Cartiva SCI Implant (01/27/2026) Abbott Spinal Cord Stimulator Lawsuit Alleges Defects Caused Lead Migration, Electric Shocks (Posted: 2 days ago) An Abbott spinal cord stimulator lawsuit filed by three women says the product was defectively designed, inappropriately approved by the FDA, and left them with severe injuries, worsening pain and the need for removal surgery. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Claims Airport Body Scanner Destroyed Woman’s Spinal Cord Stimulator, Requiring Surgical Removal (03/03/2026)Medtronic Spinal Cord Stimulator Lawsuit Filed Over Unnecessary Shocking Sensations (02/27/2026)Boston Scientific Pacemaker Lawsuit Claims Recalled Device Caused Life-Threatening Situation (02/25/2026)
Zimmer Biomet CPT Hip System Linked to Increased Risk of Thigh Bone Fractures, FDA Warns September 18, 2024
Lawyers To Nominate Hair Relaxer Cancer Cases for Early Bellwether Trials Next Week (Posted: today) Plaintiffs and defendants involved in hair relaxer cancer lawsuits are expected to turn in a list of 12 cases that the parties believe are fit to serve as bellwether trials. MORE ABOUT: HAIR RELAXER LAWSUITCourt Outlines Procedures When Women Die After Filing a Hair Relaxer Cancer Lawsuit (02/25/2026)Hair Extension Chemicals May Be More Harmful Than Previously Thought: Study (02/17/2026)MDL Judge Issues New Deadlines for Hair Relaxer Lawsuit Bellwether Trial Preparations (02/04/2026)
Cartiva Implant Recall Lawsuits Move Forward, as Plaintiffs Seek Compensation for Big Toe Surgery Failures (Posted: yesterday) Cartiva implant lawsuits are moving forward in federal court as patients across the United States seek compensation for complications linked to the recalled big toe device. MORE ABOUT: CARTIVA IMPLANT LAWSUITCartiva Synthetic Cartilage Implant Lawsuits Centralized in Federal MDL (02/10/2026)Lawsuit Alleges Cartiva Implant Loosened, Degraded in Great Toe (02/05/2026)Big Toe Fusion Lawsuit Filed Over Failed Cartiva SCI Implant (01/27/2026)
Abbott Spinal Cord Stimulator Lawsuit Alleges Defects Caused Lead Migration, Electric Shocks (Posted: 2 days ago) An Abbott spinal cord stimulator lawsuit filed by three women says the product was defectively designed, inappropriately approved by the FDA, and left them with severe injuries, worsening pain and the need for removal surgery. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Claims Airport Body Scanner Destroyed Woman’s Spinal Cord Stimulator, Requiring Surgical Removal (03/03/2026)Medtronic Spinal Cord Stimulator Lawsuit Filed Over Unnecessary Shocking Sensations (02/27/2026)Boston Scientific Pacemaker Lawsuit Claims Recalled Device Caused Life-Threatening Situation (02/25/2026)