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.
Fewer Opioids Following Hernia Repair May Be Sufficient: Study August 31, 2017 Martha Garcia Add Your CommentsPatients undergoing hernia surgery are routinely given opioid painkillers to control their pain following the operation. However, a new study indicates far fewer painkillers may be needed following hernia repair than surgeons previously believed were necessary, which should result in a re-evaluation of opioid prescriptions amid the epidemic of abuse and addiction in the United States.ย In a study published earlier this month in the medical journal Surgery, researchers from Massachusetts General Hospital and Newton-Wellesley Hospital indicated that nearly 60% of patients surveyed did not use all of the prescribed opioid painkillers following their surgery.Researchers conducted an observational study between October 1, 2015, to September 30, 2016. They included 185 hernia surgery patients from a single-surgeon, high-volume practice of hernia repair operations.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 COMPENSATIONAll patients were prescribed 10 opioid painkiller tablets, or Vicodin, postoperatively. They were also advised not to take the narcotic painkillers if they could control their pain using non-opioid painkillers, like Tylenol or Advil. Patients completed a questionnaire at their post-op appointment, about two to three weeks after surgery.In the medical community, researchers noted that it is very common for hernia patients to receive an average of 30 opioid tablets after surgery.Overall, 60% of patients said they didnโt use narcotic painkillers at all. Nearly 86% used less than 4 opioid painkiller tablets. No patients reported needing or taking opioids the week before their post-op follow-up appointment.More than half of patients completely relied on Tylenol and Advil, non-narcotic painkillers, to control their pain. These patients were less likely to have high levels of pain that were persistent. They also noted that their pain interfered less with daily activities and leisure activities than for patients who used opioids.Only 13 patients said they needed nine or more opioid tablets. Among all the patients, those who were employed and worked post-op were more likely to take opioid painkillers.About 75% reported missing more than 3 days of work, while 51% did not miss any work. About 67% of patients said the pain did not interfere with their daily lives, 23% said the pain slightly restricted their activities, and five patients said the pain significantly affected their daily activities.Researchers said the findings indicate post-operative surgery pain and how to approach the pain with opioid painkillers should be researched further, focusing on efforts to reduce the amount of narcotic painkillers prescribed to patients.While much of the attention concerning the opioid abuse epidemic has focused on the prescribing practices of primary care doctors, study authors highlighted research indicating surgeons may also play a role in opioid dependence.Opioid dependence following surgery may be as high as 6%, mainly stemming from narcotic painkillers prescribed for surgery pain. Another study found that when doctors are monitored, they prescribed fewer narcotic painkillers to patients.โThe implication of our study is that, even though surgeons have been careful to limit the number of opioid tablets that we prescribe following operations, we may still be prescribing more medication than is actually needed by our patients,โ says Peter Masiakos, MD, Department of Pediatric Surgery, MassGeneral Hospital for Children and lead author of the study. 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: Drug Abuse, Drug Overdose, Hernia, Opioids, SurgeryMore Lawsuit Stories Recalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods April 30, 2026 Weber Grill Brush Lawsuit Claims Detached Bristle Punctured Manโs Intestine April 30, 2026 AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism April 30, 2026 0 Comments X/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 Recalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (Posted: today)Insulet is removing certain Omnipod 5 insulin pump pods from use following a surge in reports of insulin delivery failures that raise risks of diabetic ketoacidosis and other serious complications.MORE ABOUT: OMNIPOD RECALL LAWSUITInsulet OmniPod 5 Recall Lawsuits May Be Filed Over Problems Resulting in Diabetic Ketoacidosis, Hospitalization and Death (03/24/2026)Omnipod 5 Insulin Pump Recall Follows Reports of Serious Injuries: FDA (03/20/2026) Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (Posted: yesterday)A Florida womanโs lawsuit alleges that Abbott Laboratories and Boston Scientific altered their SCS device batteries, firmware and stimulation features without adequate safety testing approved by the FDA.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITJPML Sets Hearing Over Spinal Cord Stimulator Lawsuit Consolidation for May 28 (04/24/2026)SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation (04/20/2026)WaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (04/14/2026) Lawsuit Blames Depo Shot for Brain Tumors, Intense Headaches (Posted: 2 days ago)A Depo-Provera lawsuit filed against Pfizer says the manufacturer knew Depo-Provera could stimulate brain tumor growth before the birth control shots hit the market, yet failed to warn doctors and patients.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Meningioma Warning Update Should Be Added to Birth Control Shot: Lawsuit (04/22/2026)Hearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (04/15/2026)High-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (04/06/2026)
AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism April 30, 2026
Recalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (Posted: today)Insulet is removing certain Omnipod 5 insulin pump pods from use following a surge in reports of insulin delivery failures that raise risks of diabetic ketoacidosis and other serious complications.MORE ABOUT: OMNIPOD RECALL LAWSUITInsulet OmniPod 5 Recall Lawsuits May Be Filed Over Problems Resulting in Diabetic Ketoacidosis, Hospitalization and Death (03/24/2026)Omnipod 5 Insulin Pump Recall Follows Reports of Serious Injuries: FDA (03/20/2026)
Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (Posted: yesterday)A Florida womanโs lawsuit alleges that Abbott Laboratories and Boston Scientific altered their SCS device batteries, firmware and stimulation features without adequate safety testing approved by the FDA.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITJPML Sets Hearing Over Spinal Cord Stimulator Lawsuit Consolidation for May 28 (04/24/2026)SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation (04/20/2026)WaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (04/14/2026)
Lawsuit Blames Depo Shot for Brain Tumors, Intense Headaches (Posted: 2 days ago)A Depo-Provera lawsuit filed against Pfizer says the manufacturer knew Depo-Provera could stimulate brain tumor growth before the birth control shots hit the market, yet failed to warn doctors and patients.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Meningioma Warning Update Should Be Added to Birth Control Shot: Lawsuit (04/22/2026)Hearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (04/15/2026)High-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (04/06/2026)