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.
Chlorpyrifos Parkinsonโs Disease Lawsuit Chlorpyrifos lawsuits are being investigated for individuals diagnosed with Parkinsonโs disease after direct, residential, occupational or Gulf War pesticide exposure.
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
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.
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.
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.
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 Nevro Stimulator Lawsuit MDL Request Opposed by Manufacturer August 14, 2026 Whippet Injuries, Deaths Lead to Bill Seeking to Ban Retail Sale of Nitrous Oxide Canisters August 14, 2026 Ninja Foodi Pressure Cooker Explosion Lawsuit Alleges Safety Defect Caused Severe Burns August 14, 2026 0 CommentsX/TwitterThis 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 Nevro Stimulator Lawsuit MDL Request Opposed by Manufacturer (Posted: today)The JPML has been asked to reject a petition by plaintiffs seeking to consolidate all federal Nevro spinal cord stimulator lawsuits before one federal judge, claiming the injuries and claims are too different from plaintiff to plaintiff.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims (08/10/2026)Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (08/06/2026)Spine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026) Gulf War Veteran Parkinsonโs Disease Lawsuits Investigated Over Pesticide Use During Operations Desert Shield and Desert Storm (Posted: yesterday)Lawyers are investigating Parkinsonโs disease lawsuits for Gulf War veterans potentially exposed to the pesticide chlorpyrifos during Operations Desert Shield and Desert Storm.MORE ABOUT: CHLORPYRIFOS PARKINSONโS DISEASE LAWSUITAgricultural Workers Face Higher Risk of ALS Due to Pesticide Exposure: Study (08/10/2026)Paraquat Exposure Lawsuit Claims Farm Herbicide Caused Parkinsonโs Disease (08/06/2026)Chlorpyrifos Pesticide Side Effects Research Highlights Decades of Parkinsonโs Disease Risks (08/04/2026) Nearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (Posted: 2 days ago)C.R. Bard and its Becton Dickinson parent company face more than 3,700 Bard PowerPort lawsuits that claim the port catheters are defectively designed.MORE ABOUT: BARD POWERPORT LAWSUITBard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)New Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026)Bard PowerPort Fracture Lawsuit Set For Second Bellwether Trial in Aug. 2026 (05/29/2026)
Whippet Injuries, Deaths Lead to Bill Seeking to Ban Retail Sale of Nitrous Oxide Canisters August 14, 2026
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Nevro Stimulator Lawsuit MDL Request Opposed by Manufacturer (Posted: today)The JPML has been asked to reject a petition by plaintiffs seeking to consolidate all federal Nevro spinal cord stimulator lawsuits before one federal judge, claiming the injuries and claims are too different from plaintiff to plaintiff.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims (08/10/2026)Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (08/06/2026)Spine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026)
Gulf War Veteran Parkinsonโs Disease Lawsuits Investigated Over Pesticide Use During Operations Desert Shield and Desert Storm (Posted: yesterday)Lawyers are investigating Parkinsonโs disease lawsuits for Gulf War veterans potentially exposed to the pesticide chlorpyrifos during Operations Desert Shield and Desert Storm.MORE ABOUT: CHLORPYRIFOS PARKINSONโS DISEASE LAWSUITAgricultural Workers Face Higher Risk of ALS Due to Pesticide Exposure: Study (08/10/2026)Paraquat Exposure Lawsuit Claims Farm Herbicide Caused Parkinsonโs Disease (08/06/2026)Chlorpyrifos Pesticide Side Effects Research Highlights Decades of Parkinsonโs Disease Risks (08/04/2026)
Nearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (Posted: 2 days ago)C.R. Bard and its Becton Dickinson parent company face more than 3,700 Bard PowerPort lawsuits that claim the port catheters are defectively designed.MORE ABOUT: BARD POWERPORT LAWSUITBard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)New Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026)Bard PowerPort Fracture Lawsuit Set For Second Bellwether Trial in Aug. 2026 (05/29/2026)