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.
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.
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.
Medpor Nose Job Implants Linked to Infections, Complications: Study August 30, 2012 Martha Garcia Add Your CommentsThe findings of a new study seem to indicate an unusually high rate of infections and complications linked to patients who have received Medpor nose job implants.ย ย Research published online August 27 by the Archives of Facial Plastic Surgery identified an increased rate of postoperative infection for nose job surgeries that used Medpor implants.The study evaluated 662 rhinoplasty surgeries, some using common skin graft and others involving the use of alloplasty implants. The procedures were performed by three faculty surgeons at the Oregon Health and Sciences University in Portland from 1999 to 2008.Do You Know about…Spinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONDo You Know AboutโฆSpinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONThe study found an incidence of postoperative infection of 2.8 percent for all 662 of the procedures. Infections occurred in roughly 20 percent of patients that underwent procedures in which Medpor implants were used.Of the 662 surgeries, Medpor or Gore-Tex implants were used in 151 of the procedures. In the cases where only Gore-Tex was used, another common implant made from expanded polytetrafluoroethylene (ePTFE) and manufactured by W.L. Gore & Associates, the infection rate was only 5.3 percent.In nearly all the procedures where either implant was used, the implant began to protrude through the nose. In procedures where surgeons grafted tissues from the patients, there were no complications.Rhinoplasty surgery, more commonly referred to as a nose job, is surgery on the nose done to change its appearance, and is sometimes completed with a common plastic implant.Medpor nose implants, manufactured by Stryker Corp. and acquired from Porex Technologies in 2010, is a product made from porous high-density polyethylene (pHDPE).Implants are often used in rhinoplasty surgery when a patient’s tissue or cartilage is unavailable from the nose, ear or ribs to graft and use for the surgery. Surgeons often prefer to graft a patients cartilage; however that takes more time than using a plastic implant.Andrew Winkler, MD, co-author of the study and plastic surgeon at the University of Colorado in Denver, noted in the study, โCaution is strongly recommended when considering the use of pHDPE in rhinoplasty.โMedpor and Gore-Tex are used for differing reasons. According to Winkler, one is soft and the other is stiff, so they are not interchangeable.An infection resulting from a nose job surgery will often lead to another surgery, in order to remove the implant. Most often, antibiotics alone will not alleviate the infection. Written by: Martha GarciaHealth & Medical Research WriterMartha Garcia is a health and medical research writer at AboutLawsuits.com with over 15 years of experience covering peer-reviewed studies and emerging public health risks. She previously led content strategy at The Blogsmith and contributes original reporting on drug safety, medical research, and health trends impacting consumers. Tags: Infection, Plastic Sugery, Stryker, Surgery InfectionMore Lawsuit Stories Dupixent Lymphoma Lawsuit Alleges Atopic Dermatitis Drug Led to Mycosis Fungoides Diagnosis August 20, 2026 Indoor Fire Pit Lawsuit Indicates Flame Jet Set User’s Body on Fire August 20, 2026 Missouri Appeals Court Orders New Trial for Similac, Enfamil NEC Lawsuit August 20, 2026 0 Comments InstagramThis 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 Dupixent Lymphoma Lawsuit Alleges Atopic Dermatitis Drug Led to Mycosis Fungoides Diagnosis (Posted: today)A California woman’s Dupixent lymphoma lawsuit claims the manufacturers knew of the eczema drug’s cancer risks, but refused to inform doctors and patients.MORE ABOUT: DUPIXENT LAWSUITDupixent CTCL Studies Highlighted Cancer Risks For Years, Lawsuit Alleges (08/11/2026)CTCL Lawsuit Alleges Diagnosis Came After Less Than a Year of Dupixent Use (07/29/2026)Lawsuit Alleges Dupixent Caused Mycosis Fungoides Diagnosis (07/21/2026) FanDuel Addiction Lawsuit Alleges Targeted Advertising Caused Substantial Gambling Losses (Posted: yesterday)A FanDuel addiction lawsuit claims a Pennsylvania man wagered massive amounts of money after being subjected to a tailored promotional campaign designed to exploit his gambling habits.MORE ABOUT: SPORTS BETTING ADDICTION LAWSUITDraftKings Predictions Lawsuit Seeks Refunds for Illegal Sports Betting Losses (08/11/2026)Class Action Lawsuit Claims DraftKings Is Dodging State Gambling Laws (07/31/2026)Lawsuit Claims FanDuel, DraftKings Caused Compulsive Gambling, Addiction and Financial Losses (07/24/2026) Boston Scientific Stimulator Lawsuit Alleges Spine Implant Caused Nerve Damage, Shocks (Posted: 2 days ago)A spinal cord stimulator lawsuit from a Kentucky man claims his Boston Scientific device was defectively designed, leaving him with permanent nerve damage and wire fragments fused into his bones.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Stimulator Lawsuit MDL Request Opposed by Manufacturer (08/14/2026)Abbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims (08/10/2026)Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (08/06/2026)
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