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.
Velveeta Recall Issued Due to Risk of Early Spoilage, Illnesses June 20, 2014 Russell Maas Add Your CommentsVelveeta cheese products distributed to certain Wal-Mart stores nationwide are being recalled, due to a lack of preservative additives, which may allow the products to spoil prematurely and potentially lead to food poisoning illnesses.A Kraft Foods Velveeta recall (PDF) was issued on June 19, following a manufacturer review of recently processed foods.It was found that about 260 cases of Velveeta distributed to Wal-Mart stores may lack sobric acid, a preservative that was supposed to be added to the food, potentially allowing them to spoil before their expiration dates.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 COMPENSATIONWhen food spoils, it causes bacteria to grow. This may cause consumers to suffer mild to severe food poisoning if the food is eaten, typically causing stomach virus symptoms within 4-48 hours, including diarrhea, stomach pain, cramping, nausea, and vomiting.The recall includes 32 ounce Kraft Velveeta original pasteurized recipe cheese products. The products were packed with 12 units per case and contain Case UPC code 10021000611611 and Consumer package UPC code 021000611614. Each unit is marked with a โBest Used Byโ date of December 17, 2014 and time stamped between 9:34 and 13:15 next to the date.The affected cheese products were manufactured by Kraft Foods and distributed to three Wal-Mart distribution centers where they were shipped to 12 Midwest states. The products were distributed directly to Wal-Mart stores in Colorado, Illinois, Indiana, Iowa, Kansas, Michigan, Minnesota, Nebraska, North Dakota, Ohio, South Dakota, and Wisconsin.Customers should not eat the recalled cheese products and return them to the Wal-Mart store they were purchased from for an exchange or a full refund. Customers may also contact Kraft Foods Consumer Relations at 1-800-310-3704 for further questions concerning the recall.Photo Courtesy of Clean Wal-Mart via Flickr CC 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.More 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 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 $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)