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.
Wrongful Death Suit Filed Over Recalled Alcohol Prep Pads July 27, 2011 Staff Writers Add Your CommentsAn Illinois widow has filed a Triad alcohol prep pad wrongful death lawsuit against H&P Industries and a number of other defendants, claiming that her husband was killed by bacteria-infected alcohol prep pads. On July 1, Sharon Rockett filed a complaint in Madison County Circuit Court against H&P Industries, Triad Group, Inc. Carefusion Corporation, the Cancer Treatment Centers of America, Inc., Genenteck Inc., and RGH Enterprises (doing business as Edgepark Medical Supplies). Rockett alleges that all of the defendants are responsible for the death of Garry W. Rockett, who died from complications caused by a bacillius cereus infection.According to allegations raised in the lawsuit, Garry Rockett received contaminated Triad alcohol prep pads in PleurX Drainage Kits, which were distributed by Carefusion and Edgepark Medical Supplies directly to the couple and through the Cancer Treatment Centers. Sharon Rockett claims that the alcohol prep pads were contaminated and that the problems should have been identified at some point along the supply chain.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 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 COMPENSATIONThe claim is the latest of several wrongful death and product liability lawsuits filed against H&P, which did business as Triad, over allegedly contaminated alcohol prep pads.H&P issued a Triad wipes recall in early January 2011, after it was discovered that prep pads, swabs and swabsticks tainted with the bacteria Bacillus cereus may have been distributed to consumers.The recalled Triad wipes, prep pads and swabs were commonly used in hospitals and packaged with a number of medications. They were also sold under variety of other labels, including CVS, Walgreens and Cardinal Health.The FDA has received at least of eight reports from doctors and patients involving deaths from Triad wipes, 11 reports of Triad wipe infections and more then 250 other problems associated with the products. However, most of the reported deaths have not involved enough evidence for investigators to truly follow up.Last month the FDA put a permanent injunction against the company doing any kind of business until it has established that its products are safe and that a number of systemic production problems have been solved. H & P indicates that it plans to meet the FDA’s requirements and re-open its business in the future. Tags: Alcohol Prep Pad, Bacillus Cereus Infection, Illinois, Product Liability, Triad, Wrongful Death Image Credit: |More Lawsuit Stories Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect June 12, 2026 Xcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis June 12, 2026 Rezurock Lawsuit Claims GVHD Medication Caused Debilitating Skin Condition, Prurigo Nodularis June 12, 2026 1 Comments Beth November 11, 2011 My father died on May 21 of this year from a blood infection contracted through his catheter. His shipment of Triad swabsticks were recalled due to contamination. 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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 Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (Posted: today)A spinal cord stimulator lawsuit claims that the Abbott Proclaim XR 5 system failed to treat a man’s 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: yesterday)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: 2 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)
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