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.
Needleless IV Connectors May Be Causing Hospital Infections, FDA Warns August 12, 2010 Staff Writers Add Your Comments Federal regulators are warning that positive displacement needleless connectors used for intravenous access may increase the risk of hospital-acquired infectionsย and death, leading to a request that manufacturers gather additional information on the potential problem.ย The FDA issued an initial communication on August 11, warning that several peer-reviewed clinical studies reported an increase in bloodstream infections once hospitals began using needle-free IV connectors that use positive displacement. The studies found that switching to other needleless connectors resulted in the infection rates dropping again. At least three deaths may be associated with positive displacement needleless connector bloodstream infections. Positive displacement needleless connectors allow multiple IV sets and catheter hubs to deliver fluids and drugs into a patient without the risk of needle stick injuries to hospital staff or patients. They are also frequently referred to as luer activated valves or positive pressure systems. Do You Know about… Spinal Cord Stimulator lawsuits Spinal 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 More SEE IF YOU QUALIFY FOR COMPENSATION Do You Know Aboutโฆ Spinal Cord Stimulator lawsuits Spinal 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 More SEE IF YOU QUALIFY FOR COMPENSATION In a letter to infection control practitioners, the FDA also announced it will require nine companies to conduct postmarket surveillance studies on positive displacement connectors to see whether they are indeed associated with higher hospital infection rates. The postmarket surveillance studies seek to answer two questions: What is the rate of bloodstream infections when that companyโs specific positive displacement needleless connectors are used, and how does that rate compare to the rates of other needleless coneectors? And are there certain patient demographics, illnesses or uses that appear to have a stronger correlation with positive displacement needleless connector bloodstream infections than others? The FDA hopes the information will allow the agency to make a more sound and fact-based recommendation on the use of the needleless systems. Concern over the systems is nothing new. In October 2008, the Society for Healthcare Epidemiologists of America and the Infectious Disease Society of America recommended against the use of positive displacement needleless connectors unless there was first a thorough assessment of the risk and benefits. The recommendations were included in a report on useful strategies in preventing bloodstream hospital infections. Tags: Hospital Infection, Infection, Medical Device Image Credit: | More Lawsuit Stories Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain April 3, 2026 Lawsuit Claims Covidien Hernia Mesh Perforated Manโs Bowel April 3, 2026 Judge Upholds $9M Crock-Pot Pressure Cooker Lawsuit Verdict April 3, 2026 2 Comments Bruce August 20, 2010 I feel that the average citizen who knows about hospital acquired infections knows essentially NOTHING about the fact that the little piece of plastic that connects the IV to the catheter in their vein, is very likely to be the CAUSE of death or morbidity. It has been overlooked by everyone for 20 years as no one thought it was a problem until Rymed technologies proved it. The entire world should be advised about reducing their risk of blood stream infections and is may be as simple as saying I demand InVision Plus IV Connector to be used on me or my family member. How many more people need to die or be injured for months or years by BAD technology? Bruce August 12, 2010 It is not only positive displacement but negative displacement devices as well. The solution to this problem is ZERO fluid motion, that is Rymed’s Invision plus technology. NOT named in the FDA warning. Check out Rymedtech.com for the solution to this horrible problem that causes over 50,000 deaths in the US alone. This does not include the morbidity of catheter related blood stream infections. Costs for both exceed 5 billion dollars a year. 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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 Term Δ MORE TOP STORIES Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (Posted: yesterday) An Illinois woman has joined a growing number of plaintiffs alleging that the Medtronic Intellis neurostimulator, and similar devices, may fail to relieve chronic pain and instead lead to worsening complications. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Spinal Cord Stimulator Lawsuits Filed Over Device Malfunction, Failure (03/30/2026)Abbott Proclaim SCS Lawsuit Alleges Stimulator Lead Migration Resulted in Multiple Surgeries (03/24/2026)Abbott, Boston Scientific Oppose Spinal Cord Stimulator Lawsuit MDL (03/20/2026) Court Outlines Plan To Prepare Suboxone Tooth Decay Lawsuits for Trial in Early 2028 (Posted: 2 days ago) Four Suboxone tooth decay lawsuits will eventually be selected and prepared for bellwether trials set to begin in March 2028, according to a court order. 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Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (Posted: yesterday) An Illinois woman has joined a growing number of plaintiffs alleging that the Medtronic Intellis neurostimulator, and similar devices, may fail to relieve chronic pain and instead lead to worsening complications. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Spinal Cord Stimulator Lawsuits Filed Over Device Malfunction, Failure (03/30/2026)Abbott Proclaim SCS Lawsuit Alleges Stimulator Lead Migration Resulted in Multiple Surgeries (03/24/2026)Abbott, Boston Scientific Oppose Spinal Cord Stimulator Lawsuit MDL (03/20/2026)
Court Outlines Plan To Prepare Suboxone Tooth Decay Lawsuits for Trial in Early 2028 (Posted: 2 days ago) Four Suboxone tooth decay lawsuits will eventually be selected and prepared for bellwether trials set to begin in March 2028, according to a court order. MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Film Lawsuit Filed by 46 Users Alleging Drug Makers Ignored Years of Dental Injury Reports (03/03/2026)100 Suboxone Film Tooth Decay Lawsuits Selected for Next Phase of Bellwether Discovery (02/13/2026)Problems With Suboxone Dental Injury Records Collection Continues in MDL (01/26/2026)
Hair Relaxer Class Action Lawsuit Seeks Certification for Medical Monitoring Claims (Posted: 3 days ago) A federal judge is being asked to certify seven hair relaxer class action lawsuits seeking medical monitoring for users, following studies that link the products to an increased risk of cancer. MORE ABOUT: HAIR RELAXER LAWSUITHair Relaxer Endometrial Cancer Lawsuits and Ovarian Cancer Lawsuits Proposed for Early Trials (03/23/2026)Lawyers To Nominate Hair Relaxer Cancer Cases for Early Bellwether Trials Next Week (03/12/2026)Court Outlines Procedures When Women Die After Filing a Hair Relaxer Cancer Lawsuit (02/25/2026)