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.
Hip, Knee Revision Surgery May Be More Likely Following Pre-Operative Opioid Use: Study August 7, 2018 Martha Garcia Add Your CommentsNew research suggests that the use of opioid painkillers before hip or knee replacement surgery is associated with a higher risk of individuals needing repeat surgery, or being readmitted to the hospital.ย In a study published last month in the Journal of Bone and Joint Surgery, researchers at the University of Chicago found that individuals were twice as likely to require another hip or knee surgery if they used a narcotic painkiller, such as Vicodin or Norco, for at least 30 days before their procedure.Researchers analyzed data for 233,000 patients in the United States who had total knee replacement and 91,000 who had total hip replacement between 2003 and 2014 using data from two Truven Health MarketScan databases. Follow-up was done for one year after surgery for all patients and three years later for 160,000 of the patients.Stay Up-to-Date Abouthip 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 hip replacement lawsuit updates or developments. "*" indicates required fieldsEmail* SIGN ME UPΔ Learn MoreStay Up-to-Date AboutHip 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 hip replacement lawsuit updates or developments."*" indicates required fieldsEmail* SIGN ME UPΔ Learn MoreMore than half of joint replacement patients had one or more opioid prescriptions filled in the six months before surgery, and about 20% of patients had prolonged opioid painkiller use before surgery.The findings indicate prolonged use of opioids, for more than 30 days, before total knee or hip replacement surgery increased a personโs risk of repeat surgery and hospitalization.Readmission rates for people who had knee replacement, but did not take narcotic painkillers was 4.8%. Comparatively the rate for those who took opioids for 60 days before surgery was 6.2%. Similarly, the readmission rates for patients who had hip replacement surgery but didn’t use opioids was 3.7%. Among those that had hip replacement surgery and used opioids for 60 days prior to surgery had readmission rates of 5.8%.After one year of follow-up, rates of repeat surgery doubled among the long-term opioid users. Those that took opioids beforehand had repeat surgery rates of 2.1%, but those who didn’t take the drugs before surgery had rates at 1%.As for the hip replacement group, the rates of repeat surgery were 0.38% for those not taking painkillers like Oxycodone or Percocet. But among users for 60 days before surgery, repeat surgery rates were 1.1%.At the three year follow-up mark, rates of readmission and repeat surgery were higher among those patients who used opioid painkillers before surgery for more than one month.Researchers warn that the findings of the new study indicate narcotic painkillers should be viewed as a risk factor for surgery, especially considering more than half of patients prescribed opioids donโt actually need them to manage their pain. Both surgeons and patients should consider the risk before opting for elective joint replacement.The findings of the new study come at a time when more than two-thirds of drug overdose deaths are caused by opioid painkillers. More people are using and abusing narcotic painkillers than ever before. A recent study found that many hip and knee replacement surgery patients are overprescribed opioids after surgery.“Although increased attention has been paid to the opioid epidemic in the U.S. in recent years, our findings highlight that opioid use should be considered yet another risk factor for surgeons and patients to consider prior to undergoing elective primary joint arthroplasty,” the researchers concluded. 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: Hip Replacement Surgery, Knee Replacement, OpioidsMore Hip Replacements Lawsuit Stories Hip Replacement Lawsuit Claims System Failure Caused Woman To Suffer โDusky Metal Diseaseโ June 5, 2026 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 0 CommentsX/TwitterThis 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 Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (Posted: 2 days ago)A spinal cord stimulator lawsuit claims that the Abbott Proclaim XR 5 system failed to treat a manโs chronic pain, instead leaving him with shocks and burning sensations.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026)Lawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (06/02/2026)Spinal Cord Stimulator Malpractice Lawsuit Claims Device Left Veteran Partially Paralyzed (05/29/2026) Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (Posted: 3 days ago)A Suboxone dental erosion lawsuit filed by nine plaintiffs accuses the manufacturer of knowing the film strips caused severe tooth decay and other oral health problems, but failed to warn the medical community or patients.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (05/20/2026)Lawsuit Alleges Suboxone Dental Damage Warnings Were Issued Too Late (05/07/2026)Study Finds No Birth Defect Risks From Suboxone When Compared to Methadone (04/30/2026) Covidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications (Posted: 4 days ago)A Covidien hernia mesh lawsuit will go before a jury next month after a federal judge rejected the manufacturer’s motion to have the case dismissed.MORE ABOUT: HERNIA MESH LAWSUITBard Ventralight Lawsuit Claims Hernia Mesh Failure Resulted in Ongoing Physical Disabilities (06/03/2026)Bard Ventralex Patch Lawsuit Claims Umbilical Hernia Mesh Failed, Requiring Removal Surgery (05/21/2026)Covidien ProGrip Mesh Complications Lawsuit Filed Over Alleged Defects and Failure To Warn Patients (04/21/2026)
Hip Replacement Lawsuit Claims System Failure Caused Woman To Suffer โDusky Metal Diseaseโ June 5, 2026
Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (Posted: 2 days ago)A spinal cord stimulator lawsuit claims that the Abbott Proclaim XR 5 system failed to treat a manโs chronic pain, instead leaving him with shocks and burning sensations.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026)Lawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (06/02/2026)Spinal Cord Stimulator Malpractice Lawsuit Claims Device Left Veteran Partially Paralyzed (05/29/2026)
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