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.
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
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.
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.
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.
AngioDynamics Port Catheter 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.
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.
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.
Dupixent Lawsuit Dupixent lawsuits are being investigated for patients who developed rare blood cancers such as cutaneous T-cell lymphoma (CTCL) after receiving injections, alleging that Sanofi and Regeneron failed to warn about the potential risks of immune suppression and delayed cancer diagnosis.
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 Supplements Undisclosed 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 Comments Federal 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 Warning The 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 lawsuits Spinal 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 More SEE IF YOU QUALIFY FOR COMPENSATION Do You Know Aboutโฆ Spinal Cord Stimulator lawsuits Spinal 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 More SEE IF YOU QUALIFY FOR COMPENSATION The 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 Investigation The 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 effects All 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 Fix After 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, Tianeptine More Lawsuit Stories Chemotherapy Injection Port Lawsuit Blames AngioDynamics SmartPort for Wrongful Death March 13, 2026 Wegovy Vision Loss Risks 5 Times Higher Than Ozempic: Study March 13, 2026 Ryobi Hedge Trimmer Lawsuit Claims Recalled Device Cut Off Tip of Woman’s Finger March 13, 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 No Post Comment I authorize the above comments be posted on this page Weekly 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 Term Δ MORE TOP STORIES Chemotherapy Injection Port Lawsuit Blames AngioDynamics SmartPort for Wrongful Death (Posted: yesterday) An infection caused by an AngioDynamics SmartPort port catheter led to the death of a woman who contracted an infection only one month after receiving the implant. MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Lawyers Outline Process for Selecting Bellwether Lawsuits in AngioDynamics MDL (03/06/2026)Port Catheter Blood Clot Results in Lawsuit Against Device Manufacturer (02/04/2026)SmartPort Infection Lawsuit Alleges AngioDynamics Catheter Defects Forced Surgical Removal (01/30/2026) Lawyers To Nominate Hair Relaxer Cancer Cases for Early Bellwether Trials Next Week (Posted: 2 days ago) Plaintiffs and defendants involved in hair relaxer cancer lawsuits are expected to turn in a list of 12 cases that the parties believe are fit to serve as bellwether trials. MORE ABOUT: HAIR RELAXER LAWSUITCourt Outlines Procedures When Women Die After Filing a Hair Relaxer Cancer Lawsuit (02/25/2026)Hair Extension Chemicals May Be More Harmful Than Previously Thought: Study (02/17/2026)MDL Judge Issues New Deadlines for Hair Relaxer Lawsuit Bellwether Trial Preparations (02/04/2026) Cartiva Implant Recall Lawsuits Move Forward, as Plaintiffs Seek Compensation for Big Toe Surgery Failures (Posted: 3 days ago) Cartiva implant lawsuits are moving forward in federal court as patients across the United States seek compensation for complications linked to the recalled big toe device. MORE ABOUT: CARTIVA IMPLANT LAWSUITCartiva Synthetic Cartilage Implant Lawsuits Centralized in Federal MDL (02/10/2026)Lawsuit Alleges Cartiva Implant Loosened, Degraded in Great Toe (02/05/2026)Big Toe Fusion Lawsuit Filed Over Failed Cartiva SCI Implant (01/27/2026)
Chemotherapy Injection Port Lawsuit Blames AngioDynamics SmartPort for Wrongful Death (Posted: yesterday) An infection caused by an AngioDynamics SmartPort port catheter led to the death of a woman who contracted an infection only one month after receiving the implant. MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Lawyers Outline Process for Selecting Bellwether Lawsuits in AngioDynamics MDL (03/06/2026)Port Catheter Blood Clot Results in Lawsuit Against Device Manufacturer (02/04/2026)SmartPort Infection Lawsuit Alleges AngioDynamics Catheter Defects Forced Surgical Removal (01/30/2026)
Lawyers To Nominate Hair Relaxer Cancer Cases for Early Bellwether Trials Next Week (Posted: 2 days ago) Plaintiffs and defendants involved in hair relaxer cancer lawsuits are expected to turn in a list of 12 cases that the parties believe are fit to serve as bellwether trials. MORE ABOUT: HAIR RELAXER LAWSUITCourt Outlines Procedures When Women Die After Filing a Hair Relaxer Cancer Lawsuit (02/25/2026)Hair Extension Chemicals May Be More Harmful Than Previously Thought: Study (02/17/2026)MDL Judge Issues New Deadlines for Hair Relaxer Lawsuit Bellwether Trial Preparations (02/04/2026)
Cartiva Implant Recall Lawsuits Move Forward, as Plaintiffs Seek Compensation for Big Toe Surgery Failures (Posted: 3 days ago) Cartiva implant lawsuits are moving forward in federal court as patients across the United States seek compensation for complications linked to the recalled big toe device. MORE ABOUT: CARTIVA IMPLANT LAWSUITCartiva Synthetic Cartilage Implant Lawsuits Centralized in Federal MDL (02/10/2026)Lawsuit Alleges Cartiva Implant Loosened, Degraded in Great Toe (02/05/2026)Big Toe Fusion Lawsuit Filed Over Failed Cartiva SCI Implant (01/27/2026)