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.
Chlorpyrifos Parkinsonโs Disease Lawsuit Chlorpyrifos lawsuits are being investigated for individuals diagnosed with Parkinsonโs disease after direct, residential, occupational or Gulf War pesticide exposure.
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.
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.
Zimmer NexGen LPS Lawsuits Filed Over Knee Replacement Problems May 9, 2011 Staff Writers Add Your CommentsIn recent weeks, at least three product liability lawsuits have been filed by individuals who experienced problems with Zimmer NexGen LPS knee replacements, alleging that they required revision surgery after the artificial replacement knee systems began to loosen or fail.ย The Zimmer NexGen LPS knee lawsuits were filed late last month in three different states by Angela Coleman, of Michigan, David R. Langevin, of Minnesota, and Barry Davis, of Kentucky.All three complaints involved knee replacements with Zimmer NexGen Legacy Posterior Stabilized (LPS) parts, which use a “high-flex” femoral component.Stay Up-to-Date AboutKnee Replacement LawsuitsAboutLawsuits.com sends a weekly digest email with information about recalls, lawsuits and warnings that may impact your family, which will include any new knee replacement lawsuit updates or developments. "*" indicates required fieldsEmail* SIGN ME UPΔ Learn MoreStay Up-to-Date AboutKnee Replacement LawsuitsAboutLawsuits.com sends a weekly digest email with information about recalls, lawsuits and warnings that may impact your family, which will include any new knee replacement lawsuit updates or developments."*" indicates required fieldsEmail* SIGN ME UPΔ Learn MoreThe Zimmer NexGen LPS “high-flex” components are designed to allow a greater degree of flexion than the standard femoral component. However, plaintiffs allege that higher flexation places the knee replacement at a higher risk of loosening.Plaintiffs indicate that the device maker created the image and impression that using the Zimmer NexGen knee was safe, despite knowledge of serious injuries associated with the components. Zimmer downplayed and understated the risk of problems with Zimmer NexGen LPS-Flex Gender Solutions, according to allegations raised in the complaints.According to a study published by The Journal of Bone and Joint Surgery (British Edition) in 2007, researchers found that 38% of individuals implanted with a Zimmer NexGen LPS-Flex total knee replacement reported loosening shortly after 2 years post implant, with more than half of those individuals requiring knee revision surgery due to pain.A Zimmer NexGen LPS recall was issued in September 2010, involving certain high-flex femoral components that were found to have nonconforming and inconsistent geometry.Over the past year, a growing number of patients throughout the United States have filed a Zimmer NexGen knee replacement lawsuit alleging that they experienced similar problems as a result of design defects associated with various components.In March 2010, concerns were raised when Dr. Richard A. Berger, a former consultant for Zimmer, presented data that suggested problems with the Zimmer NexGen CR-Flex knee resulted in the need for revision surgery in nearly 9% of cases examined and caused knee replacement loosening in more than a third of cases.Most of the complaints filed in recent months over the Zimmer knee replacements have been Zimmer NexGen CR-Flex lawsuits. However, it appears that momentum may now be growing for lawsuits involving other high-flex components by Zimmer. Tags: Kentucky, Knee Replacement, Michigan, Minnesota, Product Liability, Zimmer, Zimmer NexGen Image Credit: |More Zimmer NexGen Lawsuit Stories Zimmer NexGen Knee Replacement Bellwether Trial Ends in Defense Verdict November 9, 2015 Zimmer NexGen Knee Cases Selected for Bellwether Trials in 2015 March 28, 2014 Coordination Sought for Zimmer NexGen Knee Cases in Federal, State Cts March 14, 2014 2 Comments Cynthia September 21, 2011 I have kad twp knee replacements one in 12/04 and one in 4/10. Thefirst one cames loose and did have problems with it no strenth in upper quad standing and walking for long hrs at a time. Now i have this new one it is still the same have pain at night have pillow between knees an dno strenth in upper quad sweling . I am 52 yrs old and very active but not now have you had any problems with zimmer lcck knee replacements ? Deborah June 24, 2011 I had two knee replacement. The right one is fine. But the left one bothes me alot especially at night I have to sleep with a pillow up under my knee trying to relieve the pain.Then the doctors have run testes but can’t find anything wrong. But i’m on 60 mg morpine for my lower back. I was just taking 1 a day for a while now Im taking 2 every 12 hrs.B ecause of my knee and back..The knee surgery was suppose to be about anymore pobable. My back is another problem.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 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 Lawsuit Claims Spinal Cord Stimulator Reprogramming Caused Electric Shocks, Worsening Pain (Posted: today)Abbott faces a Proclaim spinal cord stimulator lawsuit by a man who says the device not only failed, but that he was repeatedly electrocuted when sales representatives without medical licenses tried to reprogram it.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Faces Spine Stimulator Lawsuit Brought Jointly by 17 Injured Patients (07/23/2026)Boston Scientific Spinal Cord Stimulator Lawyers to Meet With MDL Judge for Initial Conference Aug. 5 (07/16/2026)Spinal Cord Stimulator Lawsuit Claims Boston Scientific Sales Reps Made Unauthorized Device Adjustments (07/13/2026) Lawsuit Claims FanDuel, DraftKings Caused Compulsive Gambling, Addiction and Financial Losses (Posted: 3 days ago)A former FanDuel employee has filed a lawsuit against several online gambling apps, claiming they use false advertising and data collection to foster addiction in U.S. consumers.MORE ABOUT: SPORTS BETTING ADDICTION LAWSUITGambling Lawsuit Claims Illegal ‘Social Casino’ Losses Resulted in Man Becoming Homeless (07/14/2026)College Student Sports Betting May Cause Mental Health Problems: Study (07/09/2026)DraftKings Gambling Addiction Problems Caused by Intentional Algorithm Design: Lawsuit (07/01/2026) Chlorpyrifos Parkinsonโs Disease Lawsuit Claims Years of Insecticide Exposure Caused Neurological Side Effects (Posted: 5 days ago)A former pest control worker has filed a chlorpyrifos lawsuit alleging that decades of mixing and spraying the insecticide caused Parkinsonโs disease, as lawyers investigate similar claims involving routine occupational and agricultural exposure.MORE ABOUT: CHLORPYRIFOS PARKINSONโS DISEASE LAWSUITChlorpyrifos (CPF) Exposure Linked to Abnormal Brain Development in Children: Study (08/27/2025)Court Ruling Allows EPA to Proceed with Chlorpyrifos Ban (10/23/2023)New Guidance For Chlorpyrifos Pesticide Residue In Food Issued By Federal Regulators (02/14/2022)
Lawsuit Claims Spinal Cord Stimulator Reprogramming Caused Electric Shocks, Worsening Pain (Posted: today)Abbott faces a Proclaim spinal cord stimulator lawsuit by a man who says the device not only failed, but that he was repeatedly electrocuted when sales representatives without medical licenses tried to reprogram it.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Faces Spine Stimulator Lawsuit Brought Jointly by 17 Injured Patients (07/23/2026)Boston Scientific Spinal Cord Stimulator Lawyers to Meet With MDL Judge for Initial Conference Aug. 5 (07/16/2026)Spinal Cord Stimulator Lawsuit Claims Boston Scientific Sales Reps Made Unauthorized Device Adjustments (07/13/2026)
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