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.
SinuCleanse Nasal Cleanse Products Recalled Over Microbial ContaminationNasal wash recalled due to a risk that the squeeze bottles may cause dangerous blood or secondary staph infections.A recall has been issued for SinuCleanse Soft Tip Squeeze Bottle Nasal Wash Systems due to a potential contamination with Staphylococcus aureus (S. aureus) bacteria. Staphylococcus aureus are the bacteria that cause staph infections, which can lead to fevers, chills, sores, nausea, vomiting and diarrhea, potentially resulting in severe illness or death.The U.S. Food and Drug Administration (FDA) announced the SinuCleanse Nasal Wash System recall on February 25, after confirming that the product was contaminated with S. aureus, which may result in blood or secondary staph infections for users whose nasal cavity might be damaged from inflammation and injuries caused by the productโs use.Secondary infections could include endocarditis, bone and joint infections, splenic abscesses and bacterial sinusitis. They may also lead to eye tissue infections, vision problems, cranial nerve damage or meningitis, which can be fatal.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 COMPENSATIONSinuCleanse Soft Tip Squeeze Bottle Nasal Wash Systems are manufactured by Ascent Consumer Products Inc. and are used as a nasal wash to help temporarily relieve symptoms associated with sinusitis, cold, flu or allergies.The recalled products were packaged in a carton, containing a squeeze bottle and 30 saline packets.They were distributed nationwide in January 2025, through retail and online outlets, with the lot number 024122661A1 and an expiration date of December 31, 2027. The lot number and expiration date can be found on the side of the carton or on the back of the saline packets.While Ascent Consumer Products is not aware of any adverse events related to the recall, officials are warning that the products could still be in consumersโ possession.Distributors and retailers in possession of the affected products should immediately stop distributing them and remove them from their inventory. Consumers should also stop using the product immediately and either dispose of it or return it to where it was purchased.Ascent Consumer Products is notifying distributors and customers via email. Customers with questions about the recall can contact the company at cs@ascentconsumerproducts.com, Monday through Friday from 9 a.m.to 5 p.m. ET. Anybody experiencing issues related to the productโs use should consult their physician or healthcare provider. Tags: Nasal Spray, S. aureus, SinuCleanse, Staph Infection Image Credit: FDAMore Lawsuit Stories $53M Awarded to Families of Babies Who Developed NEC From Similac Special Care Formula April 10, 2026 Nurse Assist Saline Solution Lawsuit Alleges Contamination Caused Severe Infection April 10, 2026 Oster Countertop Oven Lawsuit Claims Recalled Device Caused Third Degree Burns April 10, 2026 0 CommentsURLThis 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 $53M Awarded to Families of Babies Who Developed NEC From Similac Special Care Formula (Posted: today)A jury has awarded $53 million to four mothers who say their children suffered life-altering NEC injuries from being fed Similac infant formula shortly after being born preterm.MORE ABOUT: ENFAMIL AND SIMILAC BABY FORMULA LAWSUITEnfamil Lawsuit Claims Premature Infant Required Partial Intestine Removal From NEC Side Effects (03/12/2026)High Levels of Heavy Metals Found in More Than 25 Additional Infant Formulas: Report (03/09/2026)Trial Over Similac Necrotizing Enterocolitis Injuries Underway in Chicago (03/06/2026) Vortex Port Lawsuit Filed After Port Catheter Removed Due to Infection, Blood Clots (Posted: yesterday)AngioDynamics faces a Vortex port lawsuit from a woman who says the device only lasted a month before causing an infection and dangerous blood clots in her neck.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Infection Lawsuit Claims SmartPort Defects Caused Sepsis, Pulmonary Embolism (03/23/2026)Chemotherapy Injection Port Lawsuit Blames AngioDynamics SmartPort for Wrongful Death (03/13/2026)Port Catheter Lawyers Outline Process for Selecting Bellwether Lawsuits in AngioDynamics MDL (03/06/2026) Boston Scientific Neuromodulation Lawsuit Claims Spinal Cord Stimulator Exacerbated Chronic Pain (Posted: 2 days ago)A new claim against Boston Scientific joins a growing number of spinal cord stimulator lawsuits alleging the systems have failed to relieve pain and instead worsened symptoms for many individuals.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITMedtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (04/03/2026)Nevro 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)
$53M Awarded to Families of Babies Who Developed NEC From Similac Special Care Formula April 10, 2026
$53M Awarded to Families of Babies Who Developed NEC From Similac Special Care Formula (Posted: today)A jury has awarded $53 million to four mothers who say their children suffered life-altering NEC injuries from being fed Similac infant formula shortly after being born preterm.MORE ABOUT: ENFAMIL AND SIMILAC BABY FORMULA LAWSUITEnfamil Lawsuit Claims Premature Infant Required Partial Intestine Removal From NEC Side Effects (03/12/2026)High Levels of Heavy Metals Found in More Than 25 Additional Infant Formulas: Report (03/09/2026)Trial Over Similac Necrotizing Enterocolitis Injuries Underway in Chicago (03/06/2026)
Vortex Port Lawsuit Filed After Port Catheter Removed Due to Infection, Blood Clots (Posted: yesterday)AngioDynamics faces a Vortex port lawsuit from a woman who says the device only lasted a month before causing an infection and dangerous blood clots in her neck.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Infection Lawsuit Claims SmartPort Defects Caused Sepsis, Pulmonary Embolism (03/23/2026)Chemotherapy Injection Port Lawsuit Blames AngioDynamics SmartPort for Wrongful Death (03/13/2026)Port Catheter Lawyers Outline Process for Selecting Bellwether Lawsuits in AngioDynamics MDL (03/06/2026)
Boston Scientific Neuromodulation Lawsuit Claims Spinal Cord Stimulator Exacerbated Chronic Pain (Posted: 2 days ago)A new claim against Boston Scientific joins a growing number of spinal cord stimulator lawsuits alleging the systems have failed to relieve pain and instead worsened symptoms for many individuals.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITMedtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (04/03/2026)Nevro 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)