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.
FDA Warns Some Tejocote Root Weight Loss Products Contain Poisonous Yellow OleanderYellow oleander poisoning from Tejocote Root may result in nausea, vomiting, heart problems and even death, after using certain versions of the weight loss supplements January 31, 2024 Hannah Brown Add Your CommentsFederal regulators are warning about serious health risks linked to certain weight loss dietary supplements, which are marketed as Tejocote root, but may actually be made from yellow oleander, a poisonous plant that can cause severe or even fatal poisoning.The U.S. Food and Drug Administration (FDA) issued the Tejocote warning on January 26, indicating agency investigators found multiple versions of the weight loss products that contain yellow oleander.Officials warn that the use of contaminated products may result in serious and life-threatening injuries, including neurological, gastrointestinal, and cardiovascular events. Yellow oleander is a poisonous plant native to Mexico and Central America, known among public health officials as a concerning toxic substance.Yellow Oleander Risksย Ingestion of the yellow oleander can cause adverse health effects that might be severe or fatal, according to the FDA. Symptoms of yellow oleander poisoning from Tejocote root may result in symptoms like nausea, vomiting, dizziness, diarrhea, abdominal pain, cardiac changes, and dysrhythmia.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 U.S. Centers for Disease Control and Prevention (CDC) issued a similar warning about the risks of dietary supplements containing yellow oleander in September 2023 after a 23-month-old child consumed one of the Tejocote products and suffered nausea and vomiting.However, after a few hours, the child began to experience age-specific bradycardia and hypotension. An electrocardiogram (ECG) was ordered, which showed a number of heart problems. The ECG results returned to normal after two doses of a digoxin overdose antidote were administered for cardenolide toxicity.Tejocote Root PoisoningFederal health officials began investigating Tejocote products in September 2022 after discovering the presence of yellow oleander. At the time of the initial warning, it was discovered that the products did not mention they contained yellow oleander on the labels.This latest warning was issued for 18 of the online products including; nwl NUTRA Mexican Tejocote Root, EVA NUTRITION Mexican Tejocote Root, ELV King All Natural, Tejocote Root, ELV King Tejocote Root Raiz de Tejocote, Tejocote Root Dietary Supplement Pieces, Science of Alpha Mexican Tejocote Root, Tejo Root Raiz de Tejocote, Brazil Seed, Alipotec Tejocote Root, and Raiz de Tejocote.The supplements were sold nationwide through numerous third party online platforms, including Amazon.com, Global Mix, Inc., Sunset Sales, Alipotec Raiz de Tejocote, Natural Supplements, LLC, H and Natural, Backstage CTC Seller, Innovation Natural, LLC, Pastor-Villareal, Inc., and Alipotec South TX World Green Nutrition, Inc.The FDAโs investigation is continuing, and the agency is collaborating with third-party platforms where the products were sold, which could lead to more products being added to the warning.If they have the affected products, consumers are advised to stop using them and dispose of the products immediately. The FDA calls for consumers to inform their healthcare provider even if they have, but have not used, the supplements, so that a proper evaluation can be conducted.Healthcare professionals, patients, and consumers are encouraged to report complaints, cases of exposure, and adverse events to the FDAโs MedWatch Safety Information and Adverse Event Reporting Program. Or, call their state Poison Control Center. Tags: Dietary Supplements, Poison, Tejocote, Weight Loss, Yellow OleanderMore Lawsuit Stories Lawsuit Alleges Suboxone Dental Damage Warnings Were Issued Too Late May 7, 2026 Lyft Passenger Lawsuit Alleges Rideshare Company Never Responded to Sexual Assault Claim May 7, 2026 Misha Knee System Lawsuit Alleges Defective Implant Required Second Surgery May 7, 2026 0 Comments X/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 Lawsuit Alleges Suboxone Dental Damage Warnings Were Issued Too Late (Posted: today)The makers of Suboxone continue to face lawsuits claiming that use of the opioid treatment film strips can cause severe dental damage.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITStudy Finds No Birth Defect Risks From Suboxone When Compared to Methadone (04/30/2026)Judge Says Suboxone โSchedule Aโ Lawsuits Should Be Filed Individually or Dismissed (04/27/2026)Court Outlines Plan To Prepare Suboxone Tooth Decay Lawsuits for Trial in Early 2028 (04/02/2026) Nevro Stimulator Lawsuit Alleges SCS Lead Failure Caused Nerve Damage (Posted: yesterday)A spinal cord stimulator lawsuit filed against Nevro Corporation claims two of its implants have failed in a man’s back, leaving him with nerve damage and increasing pain.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (04/29/2026)JPML Sets Hearing Over Spinal Cord Stimulator Lawsuit Consolidation for May 28 (04/24/2026)SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation (04/20/2026) Galaflex Breast Mesh Lawsuits Filed Against Becton Dickinson in Rhode Island (Posted: 2 days ago)Women nationwide have begun filing GalaFLEX breast mesh lawsuits against BD, claiming they suffered pain, permanent injuries and the need for revision surgery after the implants were used off-label for breast reconstruction.MORE ABOUT: BREAST MESH LAWSUITBreast Mesh Implant Complications Often Leave Women Asking If They Have a Lawsuit (03/05/2026)Cosmetic Surgeons Warn Against Using Internal Bra Mesh for Breast Lifts (12/11/2025)GalaFLEX Breast Mesh Problems Were Highlighted in Warnings Issued by Former Becton Dickinson Medical Director (11/14/2025)
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