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.
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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.
Target Pillowfort Weighted Blankets Recall Issued After Child Suffocation DeathsThe recall comes following reports of two young girls becoming trapped and suffocating in the blankets December 28, 2022 Russell Maas Add Your CommentsMore than 200,000 weighted blankets sold at Target Stores have been recalled, following at least two reports of children suffocating to death after becoming trapped in the heavy Pillowfort blankets.The U.S. Consumer Product Safety Commission (CPSC) announced the Target Pillowfort recall on December 22, instructing consumers to stop using the weighted blankets immediately due to the risk that young children may become trapped by unzipping and entering the blanket, which could lead to death by asphyxiation.To date, Target and the CPSC has become aware of at least four reports of children becoming trapped in the Pillowfort weighted blankets. Two of the reports included a four-year-old girl and a six-year-old girl from Camp Lejeune, North Carolina, who were killed in April 2022, after suffocating to death inside the blankets.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 recall impacts an estimated 204,000 Pillowfort Weighted Blankets measuring 60 inches long and 40 inches wide, which contain a removable and washable cover. The blankets weigh approximately six pounds and were sold in eight prints or colors including unicorn white, space navy, pink, blue, gray, buffalo plaid red, blue constellation, and unicorn pink.The recalled weighted blankets are marked with the following item numbers, which are printed on the fabric tag attached to the removable covers of the blankets.097-02-0140 (Unicorn – White)097-02-0148 (Space Navy)097-02-0361(Pink)097-02-0363 (Blue)097-02-0364 (Gray)097-02-1603 (Buffalo Plaid โ Red)097-02-3904 (Blue Constellation)097-02-3905 (Unicorn โ Pink)The Pillowfort weighted blankets were manufactured in China and sold exclusively at Target stores throughout the U.S. and online at target.com from December 2018 through September 2022 for $40.Customers are being instructed to stop using the recalled Pillowfort weighted blankets immediately and to keep them away from children. Target is offering customers a refund for the products which can be obtained by contacting the retailer atย 800-440-0680 orย by visitingย www.target.comย and navigating to the โRecall Informationโ section. Written by: Russell MaasManaging Editor & Senior Legal JournalistRussell Maas is a paralegal and the Managing Editor of AboutLawsuits.com, where he has reported on mass tort litigation, medical recalls, and consumer safety issues since 2010. He brings legal experience from one of the nationโs leading personal injury law firms and oversees the siteโs editorial strategy, including SEO and content development. Tags: Child Death, Entrapment, Suffocation, Target, Weighted Blanket RecallMore 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 FacebookThis 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)