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.
Maryland Malpractice Lawsuit Underway Over Unnecessary Heart Stents October 10, 2013 Irvin Jackson Add Your CommentsTrial is underway in Maryland state court involving a medical malpractice lawsuit against St. Joseph Medical Center and former cardiologist Mark Midei, who lost his medical license after allegedly implanting unnecessary coronary heart stents. ย The case involves a complaint filed by Glenn Weinberg, who is one of several hundred former patients of Midei who allege that they received a heart stent that was not needed. Weinberg claims that the unnecessary procedure caused him to suffer fears over the state of his health and scale back his business, costing him millions.Attorneys for Midei say that the former cardiologist diagnosed that Weinberg had suffered a small heart attack despite appearing outwardly healthy. Midei took the stand this week, claiming that his analysis of Weinberg’s health was accurate and maintaining that his actions probably saved Weinberg’s life.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 COMPENSATIONWeinberg’s complaint came after St. Joseph Medical Center in Towson, Maryland sent letters to more than 600 former Midei patients, notifying them that a subsequent review of their medical records found that they may have been implanted with a coronary heart stent that was not needed. In many cases, Midei told patients that they were suffering severe coronary blockages that required the placement of a stent, when in reality, they had only minor blockages that did not justify the treatment.Midei was stripped of his medical license in July 2011, after a federal investigation determined he had been lying to patients, telling them that they had extensive heart blockages that needed to be alleviated by coronary stent implants.Stent procedures are designed to prop open arteries that are significantly blocked, and can cost $10,000 or more. Typically it is necessary for there to be at least a 70% artery blockage for a stent implant to be considered necessary, and many patients who have received these letters were originally told that they had blockages over that amount. However, after a subsequent review of records from the procedure, many of the patients were found to have blockages that were well under 50%, which is generally considered โinsignificant.โ Some patients who received stents had blockages as low as 10%.The discovery of theย problems with unnecessary heart stents by Dr. Mideiย was first uncovered by a U.S. Justice Department (DOJ) investigation into Medicare fraud and claims of kickbacks between the hospital and the MidAtlantic Cardiovascular Associates (MACVA), of which Midei was a member at one time. He was kicked out of his position at the hospital shortly after the investigation got underway.Settlement agreements have already been reached in nearly 250 lawsuits against St. Joseph and Midei, but dozens of cases remain unresolved. As a result of the unnecessary procedures, St. Joseph also reached a $22 million settlement with the DOJ in 2010.Stent Misuse Concerns RisingThe trial comes just days after a report was issued about the overuse of coronary stents nationwide, which have been linked to serious and fatal complications in many cases.In 2012 alone, the FDA reports that at least 773 people died in cases linked to cardiac stents, representing a 71% increase since 2008. The agencyโs adverse event reporting system also logged 4,135 non-fatal stent injuries in the same year, a 33% increase over 2008. These numbers are even more troubling when considering that it is widely acknowledged that adverse events reported to the FDA only represent about 1% to 10% of all problems associated with medical devices or prescription medications.In a recent report by Bloomberg News, experts indicated that only about half of the 700,000 coronary heart stent operations each year involve the intended use for acute cases, such as restoring blood flow after a heart attack. In these cases, experts agree that they are beneficial, but many procedures each year are categorized as elective, and some estimates suggest that two-thirds of those, or more than 200,000 operations every year, are unnecessary. Written by: Irvin JacksonSenior Legal Journalist & Contributing EditorIrvin Jackson is a senior investigative reporter at AboutLawsuits.com with more than 30 years of experience covering mass tort litigation, environmental policy, and consumer safety. He previously served as Associate Editor at Inside the EPA and contributes original reporting on product liability lawsuits, regulatory failures, and nationwide litigation trends. Tags: Dr. Mark Midei, Heart Attack, Heart Surgery, Maryland, Medical Malpractice, St. Joseph Medical Center, StentMore Lawsuit Stories Covidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications June 10, 2026 SteriCare Lawsuit Claims Compromised Sterile Saline Solution Caused Manโs Death June 10, 2026 Snapchat, Roblox Lawsuit Filed by Adult Sexually Exploited as a Child June 10, 2026 0 Comments CompanyThis 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 Covidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications (Posted: today)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) Olympus Endoscope Lawsuit Filed Over ERCP Infection, Sepsis Linked to Contaminated Scope (Posted: yesterday)Lawsuit alleges Olympus failed to address known problems with sterilizing duodenoscopes, leading to a fatal ERCP infection years after federal regulators first raised concerns about the devices.MORE ABOUT: SCOPE INFECTION LAWSUITPediatric Sepsis Cases Contribute to More Than 1,800 Childrenโs Deaths Annually in U.S.: Study (03/31/2026)Infections After Colonoscopy, ERCP May Result in Lawsuits Over Olympus Scope Problems (03/27/2026) Boston Scientific Stimulator Lawsuits Centralized in Federal MDL (Posted: 2 days ago)Federal regulators have centralized at least 23 Boston Scientific spinal cord stimulator lawsuits in a multidistrict litigation that excludes multiple similar claims involving Abbott and Nevro implants.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit 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)Abbott Spinal Cord Stimulator Problems Resulted in Severe Paralysis: Lawsuit (05/19/2026)
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Olympus Endoscope Lawsuit Filed Over ERCP Infection, Sepsis Linked to Contaminated Scope (Posted: yesterday)Lawsuit alleges Olympus failed to address known problems with sterilizing duodenoscopes, leading to a fatal ERCP infection years after federal regulators first raised concerns about the devices.MORE ABOUT: SCOPE INFECTION LAWSUITPediatric Sepsis Cases Contribute to More Than 1,800 Childrenโs Deaths Annually in U.S.: Study (03/31/2026)Infections After Colonoscopy, ERCP May Result in Lawsuits Over Olympus Scope Problems (03/27/2026)
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