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.
Bentonite Me Baby Lead Poisoning Concerns Results in FDA Warning February 1, 2016 Irvin Jackson Add Your CommentsAmid concerns about a potential risk of lead poisoning, federal health regulators issued a warning late last week about a popular bentonite clay product, known as Betonite Me Baby, which reportedly contains high levels of lead.ย The FDA issued a “Benotnite Me Baby” lead poisoning warning after the Minnesota Department of Health informed the agency that the clay beauty product may expose users to lead, which is known to carry a risk of damage to the kidneys, central nervous system, and immune system.Lead exposure among children, even at low levels, may cause impaired cognitive function, reduced IQ, and behavioral difficulties.Learn More AboutLead Poisoning LawsuitsChildren diagnosed with lead poisoning after exposure to peeling or chipping lead paint in a rental home may be entitled to financial compensation and benefits.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONLearn More AboutLead Poisoning LawsuitsChildren diagnosed with lead poisoning after exposure to peeling or chipping lead paint in a rental home may be entitled to financial compensation and benefits.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONThe FDA warns that the label of Bentonite Me Baby indicates the clay can be ingested and applied topically to hair and skin. However, Alikay Naturals, the manufacturer, issued a press release saying, โAlikay Naturals is an all-natural luxury hair, skin, bath and body product line specifically advertised for topical use.โThe FDA has not confirmed any cases of lead poisoning associated with the Bentonite Me Baby product.Not For IngestionAn Alikay Naturals press release issued by the manufacturer in response to the FDA warning indicates that the initial report filed with the FDA was closed due to โconsumer alleged falsification of facts and statements.โThe Florida district of the FDA announced the office would open a separate investigation into the lead claims about the product.Alikay asserts the FDA investigated Bentonite Me Baby as a food or drug, despite advertisements that recommended the product be used topically as a detoxifier for the skin and hair, and not internally, as the FDA is stating.Rochelle Graham is the CEO of Black Onyx World, LLC and the creator of the Alikay Naturals line of beauty products, she is also a vlogger who began her career offering beauty and hair care tips on YouTube. Graham said in the press release that she has never recommended, on any company or YouTube videos, that Bentonite Me Baby be used on children or that it may be ingested internally.Alikay Naturals said the FDA tests that were conducted on the product, tested Bentonite Me Baby the same way candy and food products are tested, for internal use, not topical.The FDA recommends consumers should not purchase the product, which is sold online and in national retail stores, including Target, Sally Beauty Supply and Amazon.com. It also says anyone who has used it or given it to a child should consult their doctor.Alikay Naturals said they have not received any reports of side effects or complaints of elevated levels of lead following the FDA warning. They also plan to have the clay tested for lead by an independent laboratory.Bentonite Me Baby is made from aged volcanic ash and is marketed as a medicinal clay. Many consumers use it as a mask for both the hair and face. Other health bloggers have recommended the clay be used for both topical and internal uses to detoxify the body. However, Alikay Naturals does not support internal uses of Bentonite Me Baby. Written by: Irvin JacksonSenior Legal Journalist & Contributing EditorIrvin Jackson is a senior investigative reporter at AboutLawsuits.com with more than 30 years of experience covering mass tort litigation, environmental policy, and consumer safety. He previously served as Associate Editor at Inside the EPA and contributes original reporting on product liability lawsuits, regulatory failures, and nationwide litigation trends. Tags: Lead Poisoning, Skin CreamMore Lead Poisoning Lawsuit Stories Higher Lead Levels Linked to Decrease in Childhood Academic Performance: Study June 10, 2025 FDA Warns Some Imported Cookware Could Leach High Levels of Lead Into Food December 16, 2024 FDA Warns Additional Ground Cinnamon Products Contain High Lead Levels November 7, 2024 0 Comments CompanyThis 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 Depo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims (Posted: 2 days ago)A Depo-Provera meningioma lawsuit indicates that a woman suffered permanent and debilitating injuries after needing to have a brain tumor surgically removed.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Caused Meningioma 29 Years After First Birth Control Shots: Lawsuit (05/22/2026)Depo-Provera Lawsuit Filings Exceed 6,000, As Court Prepares for First Test Trials (05/18/2026)Intracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (05/12/2026) Dupixent Injection Lawsuit Alleges Manufacturer Failed to Warn About T-Cell Lymphoma Cancer Side Effects (Posted: 3 days ago)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: 4 days ago)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)
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