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.
Angioplasty and Heart Stents Overused By Many Cardiologists: Study July 7, 2011 Staff Writers Add Your CommentsAbout 15 percent of all cardiac stent implants and angioplasty procedures are probably unnecessary, according to the findings of a new study by U.S. researchers.ย The findings were published this week in the Journal of the American Heart Association, and come at a time when federal investigators in several states are looking into allegations that some doctors performed unnecessary heart stent implant procedures for financial gain. However, the problems with inappropriate heart stents and angioplasty procedures likely extends beyond just a few rogue doctors.Heart stents and angioplasty are procedures meant to prevent heart attacks and other cardiovascular problems in patients with clogged arteries. The procedures are collectively known as percutaneous coronary intervention (PCI).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 looked at more than 500,000 percutaneous coronary intervention procedures, and found that 15 percent of the procedures overall were likely cases where patients underwent inappropriate or questionable heart surgery.There are about 600,000 percutaneous coronary intervention procedures are performed every year in the United States, most involving stent implants.Researchers found that in cases where the patient suffered from acute conditions, nearly all of the stents were appropriate. However, in cases where patients had non-acute conditions, such as being at high risk for angina, a large number of procedures were either outright inappropriate or questionable.In recent years, a handful of doctors have come under scrutiny for performing unusually high numbers of coronary stent implants, resulting in investigations of surgeons in Maryland, Pennsylvania and Tennessee. In some of the cases, a subsequent review of the records showed that some patients barely had any signs of blocked arteries, even though doctors told them it was urgent to get a stent implanted.The most high-profile case has involved Dr. Mark Midei, who was removed from his post at St. Joseph Medical Center in Towson, Maryland after an investigation revealed that he may have implanted nearly 600 unneeded stents in patients from 2007 through mid-2009. That stent controversy has resulted in a number of stent lawsuits by patients who received the unnecessary procedures, and closer scrutiny over stent implant procedures and policies nationwide.Stents are designed to prop open arteries that are significantly blocked, costing $10,000 or more. Typically it is necessary for there to be at least a 70% artery blockage for a stent implant to be deemed necessary. However, allegations raised over implant procedures at St. Joseph and other hospitals indicate that some patients are being told they require coronary stent implants for blockages that are much less than 70% and in some cases so small as to be considered insignificant. Tags: Dr. Mark Midei, Heart Surgery, Medical Malpractice, Stent Image Credit: |||More Lawsuit Stories Lawsuit Claims Dupixent Cancer Diagnosis Occurred After Only 8 Months of Use June 17, 2026 Roblox, Snapchat, Discord Lawsuit Alleges Platforms Work in Tandem To Exploit Children June 17, 2026 Boston Scientific Pelvic Mesh Lawsuit Claims Advantage System Caused Permanent Injury, Deformity June 17, 2026 1 Comments Synthia May 4, 2014 Cardiologist within the HCA/Tri-Star network refuse to offer alternatives to angioplasty and stents. My father was implanted with stents after he told the cardiologist at Stonecrest Medical Center; Smyrna, TN that he did not want them; and wanted to speak with his daughter about the stents before they inplanted them. His daughter was never consulted. The stent implant came after he was hospitalized following a collapse; possibly due diabetic a diabetic episode. He had seen the cardiologist int he past few weeks for edema, and the medications prescribed seemed to be helping the situation. Two weeks prior to the stent implant, my father had heart tests, and the doctor stated that everything looked good; all chambers working fine, and NO blockages. So within exactly 14 days, he went from no blockages, to multiple blockages, and a stent procedure. On the paperwork that is signed for the angiogram, there is a small print that states “Other procedures as deemed necessary based on findings”. This verbiage is where an angiogram becomes a stent implant…it’s a racket for additional money for HCA/Tri-Star. 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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 Dupixent Cancer Diagnosis Occurred After Only 8 Months of Use (Posted: today)The makers of Dupixent face a CTCL lawsuit by a man who says he developed the rare form of cancer less than a year after beginning treatment with the eczema drug.MORE ABOUT: DUPIXENT LAWSUITRezurock Lawsuit Claims GVHD Medication Caused Debilitating Skin Condition, Prurigo Nodularis (06/12/2026)Dupixent Injection Lawsuits Consolidated in MDL Over CTCL Diagnoses (06/09/2026)Dupixent Injection Lawsuit Alleges Manufacturer Failed to Warn About T-Cell Lymphoma Cancer Side Effects (06/04/2026) Abbott Spinal Cord Stimulator Battery Problems Led to Repeat Surgeries, Lawsuit Claims (Posted: yesterday)Four plaintiffs allege Abbott spinal cord stimulator battery problems, painful malfunctions and other device failures caused worsening symptoms and repeat surgeries after the company made hundreds of changes to its implant systems.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (06/12/2026)Boston 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) Depo-Provera Lawsuit Settlement Agreement May Resolve Eligible Meningioma Claims in MDL (Posted: 2 days ago)A tentative Depo-Provera lawsuit settlement has been announced, vacating the start of the first bellwether trial while details are finalized.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims (06/05/2026)Depo-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)
Boston Scientific Pelvic Mesh Lawsuit Claims Advantage System Caused Permanent Injury, Deformity June 17, 2026
Lawsuit Claims Dupixent Cancer Diagnosis Occurred After Only 8 Months of Use (Posted: today)The makers of Dupixent face a CTCL lawsuit by a man who says he developed the rare form of cancer less than a year after beginning treatment with the eczema drug.MORE ABOUT: DUPIXENT LAWSUITRezurock Lawsuit Claims GVHD Medication Caused Debilitating Skin Condition, Prurigo Nodularis (06/12/2026)Dupixent Injection Lawsuits Consolidated in MDL Over CTCL Diagnoses (06/09/2026)Dupixent Injection Lawsuit Alleges Manufacturer Failed to Warn About T-Cell Lymphoma Cancer Side Effects (06/04/2026)
Abbott Spinal Cord Stimulator Battery Problems Led to Repeat Surgeries, Lawsuit Claims (Posted: yesterday)Four plaintiffs allege Abbott spinal cord stimulator battery problems, painful malfunctions and other device failures caused worsening symptoms and repeat surgeries after the company made hundreds of changes to its implant systems.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (06/12/2026)Boston 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)
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