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.
CDC Detects Synthetic Cannabinoids, THC in Recalled Neptune’s Fix SupplementsUndisclosed chemicals in recalled Neptune’s Fix supplements could cause serious health side effects, such as those reported among some users of the “gas station heroin” February 5, 2024 Katherine McDaniel Add Your CommentsFederal health officials indicate that Neptuneโs Fix products sold at convenience stories nationwide, which are commonly referred to as “gas station heroin”, appear to contain several potentially harmful substances, which may be responsible for serious and life-threatening health side effects reported among users the recalled dietary supplement.In findings published last week in the U.S. Centers for Disease Control and Prevention (CDC) Morbidity and Mortality Weekly Report (MMWR), researchers report that they detected synthetic cannabinoids, and other likely dangerous additives in recalled Neptune’s Fix products.Neptuneโs Fix was marketed as a dietary supplement to improve brain function, anxiety, depression, pain, and opioid use disorder. It contains the drug tianeptine, which is an opioid receptor that is prescribed as an antidepressant in some other countries, but has not been approved for medical use in the U.S.Although tianeptine in Neptune’s Fix produces opioid-like effects, it has been widely available at gas stations until recently.Neptuneโs Fix Recall and WarningThe FDA announced a Neptuneโs Fix recall on January 29, after an investigation revealed the product was linked to reports of overdoses, seizures, loss of consciousness, and suicidal behavior.The recall impacted all of Neptune’s Fix products, including elixirs, extra strength elixirs, and tablets, and was issued only a week after the FDA warned about potentially life-threatening side effects of Neptune’s fix. In the warning, the FDA indicated that consumers with a history of opioid use disorder or dependency may face a higher risk of becoming addicted to the dietary supplement. Abuse and misuse of tianeptine could also result in coma or death, the FDA indicated in the warning first released on January 23.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 FDA has issued also issued a number of prior warnings about potential health risks associated with tianeptine. In 2018, the agency indicated that tianeptine exposure had been associated with a growing number of serious side effects, including addiction. Another tianeptine warning issued in 2022 urged consumers to avoid using Coaxial, Stablon or Tianna supplements containing tianeptine that were being illegally marketed as a dietary supplement to treating various ailments, which are not approved by the FDA.Neptuneโs Fix InvestigationThe CDC investigation began after a New Jersey poison control database suggested there were more than 20 tianeptine exposure calls from healthcare facilities between June 17 and November 6, 2023, compared to normal rates of two or less tianeptine exposure calls per year.Among the 17 consumers who experienced problems, 14 reported they ingested Neptuneโs Fix containing tianeptine and kavain, another sedating dietary supplement extracted from the kava plant. Nine patients reported they had previously used tianeptine, and six reported they had consumed other substances with tianeptine, such as sedatives, antidepressants, anticonvulsants, synthetic opioids, and herbal substances with opioid-like effectsAll individuals were admitted to a medical facility with altered mental states after consuming tianeptine. According to the report, 11 patients suffered abnormally fast heart rates, 10 experienced dangerously low blood pressure, eight suffered seizures, seven experienced irregular heart rhythms, four experienced delayed heartbeats, and one suffered cardiac arrest. In addition, 13 patients were admitted to an intensive care unit, and seven underwent endotracheal intubation; an emergency medical procedure required for those who are unconscious, or cannot breathe on their own.While no deaths were reported among the patients, CDC researchers indicate the irregular heart rhythms and delayed heartbeats are known to be associated with an increased risk of developing ventricular arrhythmias; abnormal heart rhythms that make the lower chambers of your heart twitch instead of pump.Synthetic CBD Found in Neptune’s FixAfter the CDC initiated its investigation, researchers tested samples of both opened and unopened bottles of Neptuneโs Fix products obtained from two patients who experienced serious side effects.According to the report, the researchers found several other ingredients in the six samples they analyzed that were not disclosed on the products’ labels. Testing revealed the products contained cannabidiol (CBD) and tetrahydrocannabinol (THC), both psychoactive ingredients found in cannabis plants. CDC investigators also detected potentially harmful synthetic marijuana cannabinoids ADB-4en-PINACA and MDMB-4en-PINACA.The researchers warned that the health risks associated with artificially made cannabinoids are not well known, however, they have been shown to be highly potent in vitro, and have been identified in autopsy toxicology testing.CDC officials call for the public and healthcare professionals to be aware of the health risks associated with unapproved tianeptine, which has been sold under the product names Neptuneโs Fix, Pegasus, and Zaza. They also warn consumers to be mindful that these products may be adulterated with other undisclosed ingredients, which may produce serious and unexpected side effects or drug dependency. Tags: Antidepressant, Coma, Dietary Supplements, Drug Recall, Neptune's Fix, Seizures, Synthetic Cannabis, THC, TianeptineMore Lawsuit Stories Recalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods April 30, 2026 Weber Grill Brush Lawsuit Claims Detached Bristle Punctured Manโs Intestine April 30, 2026 AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism April 30, 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 Recalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (Posted: today)Insulet is removing certain Omnipod 5 insulin pump pods from use following a surge in reports of insulin delivery failures that raise risks of diabetic ketoacidosis and other serious complications.MORE ABOUT: OMNIPOD RECALL LAWSUITInsulet OmniPod 5 Recall Lawsuits May Be Filed Over Problems Resulting in Diabetic Ketoacidosis, Hospitalization and Death (03/24/2026)Omnipod 5 Insulin Pump Recall Follows Reports of Serious Injuries: FDA (03/20/2026) Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (Posted: yesterday)A Florida womanโs lawsuit alleges that Abbott Laboratories and Boston Scientific altered their SCS device batteries, firmware and stimulation features without adequate safety testing approved by the FDA.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITJPML 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)WaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (04/14/2026) Lawsuit Blames Depo Shot for Brain Tumors, Intense Headaches (Posted: 2 days ago)A Depo-Provera lawsuit filed against Pfizer says the manufacturer knew Depo-Provera could stimulate brain tumor growth before the birth control shots hit the market, yet failed to warn doctors and patients.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Meningioma Warning Update Should Be Added to Birth Control Shot: Lawsuit (04/22/2026)Hearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (04/15/2026)High-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (04/06/2026)
AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism April 30, 2026
Recalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (Posted: today)Insulet is removing certain Omnipod 5 insulin pump pods from use following a surge in reports of insulin delivery failures that raise risks of diabetic ketoacidosis and other serious complications.MORE ABOUT: OMNIPOD RECALL LAWSUITInsulet OmniPod 5 Recall Lawsuits May Be Filed Over Problems Resulting in Diabetic Ketoacidosis, Hospitalization and Death (03/24/2026)Omnipod 5 Insulin Pump Recall Follows Reports of Serious Injuries: FDA (03/20/2026)
Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (Posted: yesterday)A Florida womanโs lawsuit alleges that Abbott Laboratories and Boston Scientific altered their SCS device batteries, firmware and stimulation features without adequate safety testing approved by the FDA.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITJPML 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)WaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (04/14/2026)
Lawsuit Blames Depo Shot for Brain Tumors, Intense Headaches (Posted: 2 days ago)A Depo-Provera lawsuit filed against Pfizer says the manufacturer knew Depo-Provera could stimulate brain tumor growth before the birth control shots hit the market, yet failed to warn doctors and patients.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Meningioma Warning Update Should Be Added to Birth Control Shot: Lawsuit (04/22/2026)Hearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (04/15/2026)High-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (04/06/2026)