Dupixent Injection Lawsuit Alleges Manufacturer Failed to Warn About T-Cell Lymphoma Cancer Side Effects
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.
Contact Lens Risks Are Focus of FDA Safety Recommendations February 29, 2016 Martha Garcia Add Your CommentsFederal regulators recently updated recommendations for consumers to increase the safety of contact lenses and contact lens solutions, urging consumers to only use the products exactly as recommended by manufacturers.ย The FDA update on contact lens safety, which was revised on February 26, highlights the importance of understanding the risks associated with contact lens, including potentially serious eye infections corneal abrasions and even blindness.Approximately 40 million Americans wear contact lenses, and the FDA indicates that between 40% and 90% of wearers do not properly follow the care instructions, increasing their risk of problems.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 COMPENSATIONContact lenses are designed to offer consumers flexibility, convenience, and a โno-glassesโ appearance. They help correct a variety of vision disorders, including nearsightedness, farsightedness, astigmatism and poor focusing. However, with the lenses worn directly on the eyes, they can lead to a number of potential health risks.The FDA warns that the best strategy for reducing the risk of infection is proper hygiene, cleaning and care of the lenses. Following all product labeling and instructions for disinfection and storing. Other ways to prevent infection is to follow recommended lens wearing schedules and by having routine eye exams.There are several types of contact lenses available for consumers to purchase, including soft contacts, prescribed with a frequent replacement schedule from one day, two weeks, to a year; rigid gas permeable (RGP), which generally allow for clear, crisp vision, last longer than soft contacts, and are less likely to tear; as well as extended wear contacts that are designed for overnight or continuous wear, ranging from one to six nights or up to 30 days.Other types include, disposable contacts, which are used once and discarded, a brand new pair of lenses is used each day; Ortho-K or Orthokeratology are RGP lenses specially fitted to change the curvature of the cornea to temporarily improve the eyes ability to focus. The FDA requires that eye care professionals be trained and certified before using these lenses in their practices; as well decorative contacts, which are costume colored fashion lenses that do not correct vision and are intended to change the appearance of the eye.A 2013 study concluded the pigments in colored contacts may easily come off and decorative contacts may also be more susceptible to microorganisms than prescription contacts. The agency warns users should get a valid prescription for any type of contact lens, as they are not one size fits all.Also, when getting an exam make sure to the get a copy of the prescription. It should have information about the type of material, manufacturer, base curve, or diameter when appropriate. Always make sure to purchase the lenses with a valid prescription from valid pharmacies, optical retailers, and online retailers. Be cautious when buying from someone other than your eye care professional, they are not over-the-counter devices.Contact Lens TipsThe FDA recommends that consumers make sure to replace the contact lens storage case at least every 3 months, and always use the new contact lens case that comes with each box, and follow all directions that are included or inside packaging. Always remove lenses before swimming and never reuse solution.Never use water to clean the lenses, which can be a source of microorganisms that may cause serious eye infections and never transfer the solution from the container to another smaller container. The solution is sold in sterile containers to reduce living germs and microorganisms.Solutions that contains hydrogen peroxide require special care. Never put that solution directly into eyes, as it may cause stinging, burning, and damage to the cornea. You must follow with a neutralizer, always sold with hydrogen peroxide kit, which turns the peroxide into water and oxygen to make it safe to put in eyes. It must also be left in the neutralizer for at least 6 hours for the process to finish.The FDA also advises that consumers never ignore symptoms of eye irritation or infection associated with wearing contacts, including discomfort, excess tearing, discharge, unusual sensitivity to light, itching, burning, gritty feelings, unusual redness, blurred vision, swelling and pain. Written by: Martha GarciaHealth & Medical Research WriterMartha Garcia is a health and medical research writer at AboutLawsuits.com with over 15 years of experience covering peer-reviewed studies and emerging public health risks. She previously led content strategy at The Blogsmith and contributes original reporting on drug safety, medical research, and health trends impacting consumers. Tags: Contact Lens, Contact Lens Solution, Infection, Vision LossMore Lawsuit Stories Dupixent Injection Lawsuit Alleges Manufacturer Failed to Warn About T-Cell Lymphoma Cancer Side Effects June 4, 2026 Hair Dye Bladder Cancer Lawsuit Indicates Salon Products Contributed to Cosmetologistโs Diagnosis June 4, 2026 Addictive Video Games Left 12 Year Old With Neurological Harm, Lawsuit Claims June 4, 2026 0 Comments NameThis 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 Dupixent Injection Lawsuit Alleges Manufacturer Failed to Warn About T-Cell Lymphoma Cancer Side Effects (Posted: today)Regeneron and Sanofi-Aventis face a Dupixent injection lawsuit from a Louisiana woman who says the companies knew about the drug’s risks but downplayed them to doctors and patients.MORE ABOUT: DUPIXENT LAWSUITDupixent Cancer Lawsuit Claims Eczema Drug Caused Womanโs CTCL Diagnosis (05/28/2026)Link Between Dupixent and Cancer Withheld From Doctors and Users, Lawsuit Alleges (05/11/2026)Lawsuit Indicates Dupixent Lymphoma Diagnosis Resulted in Multiple Rounds of Chemotherapy (05/01/2026) Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (Posted: yesterday)A Nevada woman has filed a lawsuit alleging defects in AngioDynamicsโ port catheters caused her Xcela device to trigger a thrombosis in her right internal jugular vein.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITSmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body (05/15/2026)18 AngioDynamics Port Catheter Lawsuits Will Be Selected for Bellwether Discovery in August 2026 (05/05/2026)AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism (04/30/2026) Lawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (Posted: 2 days ago)According to a man’s lawsuit, the failure of spinal cord stimulator device leads caused him to require revision surgery that resulted in heart problems and permanent health complications.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITSpinal 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)Abbott Eterna Lawsuit Alleges Spinal Cord Stimulator Malfunction Resulted in Worsening Pain (05/13/2026)
Dupixent Injection Lawsuit Alleges Manufacturer Failed to Warn About T-Cell Lymphoma Cancer Side Effects June 4, 2026
Hair Dye Bladder Cancer Lawsuit Indicates Salon Products Contributed to Cosmetologistโs Diagnosis June 4, 2026
Dupixent Injection Lawsuit Alleges Manufacturer Failed to Warn About T-Cell Lymphoma Cancer Side Effects (Posted: today)Regeneron and Sanofi-Aventis face a Dupixent injection lawsuit from a Louisiana woman who says the companies knew about the drug’s risks but downplayed them to doctors and patients.MORE ABOUT: DUPIXENT LAWSUITDupixent Cancer Lawsuit Claims Eczema Drug Caused Womanโs CTCL Diagnosis (05/28/2026)Link Between Dupixent and Cancer Withheld From Doctors and Users, Lawsuit Alleges (05/11/2026)Lawsuit Indicates Dupixent Lymphoma Diagnosis Resulted in Multiple Rounds of Chemotherapy (05/01/2026)
Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (Posted: yesterday)A Nevada woman has filed a lawsuit alleging defects in AngioDynamicsโ port catheters caused her Xcela device to trigger a thrombosis in her right internal jugular vein.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITSmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body (05/15/2026)18 AngioDynamics Port Catheter Lawsuits Will Be Selected for Bellwether Discovery in August 2026 (05/05/2026)AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism (04/30/2026)
Lawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (Posted: 2 days ago)According to a man’s lawsuit, the failure of spinal cord stimulator device leads caused him to require revision surgery that resulted in heart problems and permanent health complications.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITSpinal 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)Abbott Eterna Lawsuit Alleges Spinal Cord Stimulator Malfunction Resulted in Worsening Pain (05/13/2026)