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.
Patients Face Increased Risk of Death During Hospital Staff Rotations: Study December 8, 2016 Martha Garcia Add Your CommentsNew research suggests that hospitalized patients may face an increased likelihood of death when there is a shift change, raising questions about recent restrictions for on-duty hours among residents.ย In a study published this week in the Journal of the American Medical Association (JAMA), researchers found overall patients who were cared for during hospital staff rotations had a higher mortality, as well as at 30 and 90 days after discharge.The multi-center cohort study was conducted at 10 university-affiliated U.S. Veterans Health Administration Hospitals from 2008 to 2014. More than 230,000 patients were admitted to internal medicine services during that time.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 COMPENSATIONNearly 26,000 patients had intern-only end-of-rotation transitions, more than 26,000 had resident-only end-of-rotation transitions, and about 11,000 had transitions with both interns and residents. Patients were included that died or were discharged within seven days after transition. These were compared to all other patients discharged.Overall, end-of-rotation staff transitions in care, known as patient hand-offs, were associated with significantly higher in-hospital mortality.The death rate was 3.5 percent for intern only transitions compared to two percent for the control group. Comparatively, the mortality rate for intern and resident transition was four percent compared to 2.1 percent for the control group. The resident-only group had less of a difference at 3.3 percent mortality versus the two percent hospital rate.Researchers determined the mortality rate for other patients staying in the hospital was two percent, and the mortality rate at 30 days discharge was 9.45 percent, and 14.43 percent at 90 days.The adjusted 30 day mortality rate was higher in all transition groups compared to the control rate. The intern transition group had a mortality rate of 14.5 percent compared to the control at 8.8 percent. The resident only groupโs death rate was 13.8 compared to 8.9, and the intern and resident groups had a mortality rate of 15.5 percent compared to 9.1.Even the morality rates at 90 days were much higher for all three transition groups.The intern only group had a 90 day mortality rate of 21.5 percent compared to 13.5 percent, the resident only groupโs death rate was 20.9 percent compared to 13.6 percent, and the intern and resident group had a death rate of 22.8 percent compared to 14 percent for the control group.Researchers said the maximum on-duty hour regulations implemented by the Accreditation Council for Graduate Medical Education (ACGME) have a strong association with increased death rates for end-of-shift care for both the intern only and intern and resident groups, but not for controls.โEnd-of-rotation transition in care was associated with significantly higher in-hospital mortality,โ wrote study authors. โThe association was stronger following institution of ACGME duty hour regulations.โHospital Workshift ConcernsIn 2011, the ACGME mandated a 16-consecutive hour cap on shifts for first year residents, a 28 hour cap on shifts for all other residents, and a minimum 8 hour time off between work shifts for all residents. The rules were put in place to protect patients and reduce the risk of medical mistakes caused by fatigue, which have been shown to be 10 times more prevalent than previously believed.Multiple physician groups have lobbied against these regulations, calling for a rollback of elements of ACGME restrictions. These critics say limits may actually increase the rate of medical errors, by increasing the frequency of patient handoffs between medical residents.In 2014, a study concluded patient handoff errors can be addressed using the I-PASS program, which researchers found reduced can reduce the risk of serious and potentially life-threatening medical errors by 23% and injuries due to medical errors by 30%, while improving patient care.However, the consumer watchdog group, Public Citizen, has warned that weakening resident work hour restrictions may lead to residents working without adequate sleep and threatens the health of residents and patients. The group cites evidence that shows sleep deprivation, due to excessively long work shifts, increases the risk of motor vehicle accidents, depression, needle-stick and other injuries that expose residents to blood-borne pathogens. It also exposes patients to increased risk of medical errors, leading to injury and death.The only rigorous trial to date concludes reducing shifts to 16 hours or less helped to reduce the frequency of serious medical errors, the group says. 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: Hospital, Medical MistakeMore Lawsuit Stories Depo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims June 5, 2026 New Trial Sought for First Bard PowerPort Bellwether Lawsuit June 5, 2026 Hip Replacement Lawsuit Claims System Failure Caused Woman To Suffer โDusky Metal Diseaseโ June 5, 2026 0 Comments EmailThis 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 Depo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims (Posted: 2 days ago)A Depo-Provera meningioma lawsuit indicates that a woman suffered permanent and debilitating injuries after needing to have a brain tumor surgically removed.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Caused Meningioma 29 Years After First Birth Control Shots: Lawsuit (05/22/2026)Depo-Provera Lawsuit Filings Exceed 6,000, As Court Prepares for First Test Trials (05/18/2026)Intracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (05/12/2026) Dupixent Injection Lawsuit Alleges Manufacturer Failed to Warn About T-Cell Lymphoma Cancer Side Effects (Posted: 3 days ago)Regeneron and Sanofi-Aventis face a Dupixent injection lawsuit from a Louisiana woman who says the companies knew about the drug’s risks but downplayed them to doctors and patients.MORE ABOUT: DUPIXENT LAWSUITDupixent Cancer Lawsuit Claims Eczema Drug Caused Womanโs CTCL Diagnosis (05/28/2026)Link Between Dupixent and Cancer Withheld From Doctors and Users, Lawsuit Alleges (05/11/2026)Lawsuit Indicates Dupixent Lymphoma Diagnosis Resulted in Multiple Rounds of Chemotherapy (05/01/2026) Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (Posted: 4 days ago)A Nevada woman has filed a lawsuit alleging defects in AngioDynamicsโ port catheters caused her Xcela device to trigger a thrombosis in her right internal jugular vein.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITSmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body (05/15/2026)18 AngioDynamics Port Catheter Lawsuits Will Be Selected for Bellwether Discovery in August 2026 (05/05/2026)AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism (04/30/2026)
Depo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims June 5, 2026
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Depo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims (Posted: 2 days ago)A Depo-Provera meningioma lawsuit indicates that a woman suffered permanent and debilitating injuries after needing to have a brain tumor surgically removed.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Caused Meningioma 29 Years After First Birth Control Shots: Lawsuit (05/22/2026)Depo-Provera Lawsuit Filings Exceed 6,000, As Court Prepares for First Test Trials (05/18/2026)Intracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (05/12/2026)
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Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (Posted: 4 days ago)A Nevada woman has filed a lawsuit alleging defects in AngioDynamicsโ port catheters caused her Xcela device to trigger a thrombosis in her right internal jugular vein.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITSmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body (05/15/2026)18 AngioDynamics Port Catheter Lawsuits Will Be Selected for Bellwether Discovery in August 2026 (05/05/2026)AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism (04/30/2026)