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.
Strangulation Deaths Lead to Window Shades and Blinds Recalls August 27, 2009 AboutLawsuits Add Your CommentsThe deaths and injuries of several children have led to a number of recalls for window blinds and shades sold at Target, IKEA, Pottery Barn and other retailers.The U.S. Consumer Product Safety Commission (CPSC) announced the window shade and blind recalls on August 26, affecting more than 5.4 million units. All of the recalls were issued due to the risk that children may become entangled and strangle themselves.At least three deaths and several near strangulation reports have been attributed to design defects with the recalled products, involving cords, beaded chains or drawstrings that can become looped around a childโs neack.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 COMPENSATIONThe recalls include:Target Roman Shades and Oval Roll-Up Blinds Recall: Approximately 4.2 million roll-up blinds and 600,000 Roman shades sold exclusively at Target stores. The Woolrich Roman Shades have two head rail labels that read โLewis Hyman, Inc., www.lewishymaninc.comโ and โLHI, 005301, Made in China.โ They were sold between March 2006 and December 2008. The 1/4″ Oval roll-up blinds, which do not have a release clip, have a โLewis Hyman, Inc.โ label and the year of manufacture on the bottom rail, along with a warning against possible strangulation. They were sold between January 2009 and December 2003.Ikea MELINA Roman Blinds Recall: Approximately 120,000 MELINA Roman Blinds sold exclusively at Ikea, which have a sewn-in label at the top edge with the IKEA logo and the article name (MELINA). They also have a five-digit supplier number, 19395 and a four-digit date stamp and the words โMade in Taiwan.โ They were sold between August 2006 and June 2008.Pottery Barn Kids Roman Shades Recall: Approximately 85,000 roman shades with exposed inner cords on the back have been recalled. They all have โpottery barn kidsโ on a label at the bottom edge of the shade and another label warning of the risk of strangulation. Roman shades with a fabric covering on the cords are not being recalled. They were sold between January 2003 and May 2007.Roller Shades Recall: About 245,000 roller shades distributed by Lutron Electronics Co. Inc., which includes custom-ordered shades that have an adhesive strip connecting the shade to the roller tube and reads โLutron Shading Solutionsโ and โ800-446-1503.โ They were sold through specialty dealers and Expo Design Centers between January 2000 and April 2009.Target Thermal Sailcloth and Matchstick Bamboo Roman Shade Recall: Approximatey 163,00 shades imported by Victoria Classics, including brown Matchstick roman shades and thermal shades sold in coffee, red, ivory and tan colors. They were sold exclusively at Target and through Target.com between September 2008 and June 2009.Vertical Land Blind and Shade Recall: Approximately 15,400 horizontal blinds, 16,400 vertical blinds and 800 cellular shades sold at Vertical Land stores in Panama City and Pensacola, Florida. The custom-made vertical and cellular window coverings that lack a cord tensioning device, and the horizontal blinds do not have inner cord stop devices. They were sold between January 1992 and December 2006.The CPSC urges consumers to cease using these products immediately. They can contact the various manufacturers for refunds, vouchers and replacement kits. Tags: Blinds, Ikea, Roman Shades, TargetMore 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 EmailThis 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)