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 Additional Ground Cinnamon Products Contain High Lead Levels Because of the long shelf life for ground cinnamon, the FDA advises consumers to check for any potentially toxic versions of the spice in their home and throw it out immediately. November 7, 2024 Martha Garcia Add Your Comments Federal regulators have identified several more brands of ground cinnamon that may be contaminated with high levels of lead, which could cause serious and life-altering injuries, especially for developing children. Over the past year, the U.S. Food and Drug Administration (FDA) has identified a number of problems with ground cinnamon containing dangerous levels of lead, which is a toxic metal that is known to cause a wide range of health issues, including damage to the brain and nervous system, reproductive health and other side effects. In an FDA safety alert issued on November 1, the agency indicates that testing has confirmed ground cinnamon sold under the Super Brand and Asli labels should be added to the long list of cinnamon products that may contain toxic levels of lead, urging families to check their pantry and immediately throw them away. Ground Cinnamon Lead Contamination Concerns The agency first became aware of widespread lead contamination in cinnamon products following the WanaBana fruit pouch recall issued at the end of 2023. The FDA announced the recall after testing identified high lead concentrations in several batches of the cinnamon-flavored applesauce product, which was widely marketed for use by children. More than 500 cases of lead poisoning were linked to the contaminated apple sauce, and a federal investigation determined the lead entered the products from a ground cinnamon supplier, who intentionally added excessive amounts of lead to the spice to increase their profits. In July 2024, the FDA issued a lead poisoning alert for El Servidor ground cinnamon products, which were sold throughout the state of New York. The agency then issued a larger lead contamination alert for six other brands of cinnamon products, which were found to contain dangerous levels of lead. Following the recalls, an investigation conducted by Consumer Reports found that one-third of all cinnamon products they sampled from stores across the northeastern U.S. were tainted with toxic levels of lead, which could pose health risks for children and other consumers. Learn More About Lead Poisoning Lawsuits Children 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 More SEE IF YOU QUALIFY FOR COMPENSATION Learn More About Lead Poisoning Lawsuits Children 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 More SEE IF YOU QUALIFY FOR COMPENSATION Lead is a heavy metal that is known to be toxic to the human body. Symptoms of lead exposure may include vomiting, fatigue, seizures, tremors, weight loss and other potential side effects. However, for children, lead exposure can change the structural integrity of the brain, leading to permanent cognitive problems, lower IQ scores, behavioral problems and other issues. The American Academy of Pediatrics has warned there is no safe level of lead exposure for children, and exposure even at low levels can lead to serious injuries, including delayed growth, coma, convulsions and death. Super Brand and Asli Ground Cinnamon Warning The new FDA alert indicates that Super Brand and Asli brand ground cinnamon products have also been found to contain high levels of toxic lead, after samples collected by the Arkansas Department of Health confirmed the presence of the toxic metal. The FDA warns that these products may be unsafe for consumer use and the agency has recommended that the company issue a voluntary recall. However, in the meantime, the agency is urging consumers to immediately stop using the affected cinnamon and throw away any of the unused products. Cinnamon has a long shelf life, so consumers should check their homes for the product and make sure that it is not used. The FDA indicates that it is continuing to analyze various different ground cinnamon products and review samples for elevated levels of lead. If someone may have been exposed to the tainted cinnamon, the FDA indicates that they should immediately contact a doctor. Written by: Martha Garcia Health & Medical Research Writer Martha Garcia is a health and medical research writer at AboutLawsuits.com with over 15 years of experience covering peer-reviewed studies and emerging public health risks. She previously led content strategy at The Blogsmith and contributes original reporting on drug safety, medical research, and health trends impacting consumers. Tags: Cinnamon, Cinnamon Recall, Lead Exposure, Lead Poisoning More 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 Biden Announces Funding To Replace Lead Water Pipes in U.S. Over Next 10 Years October 9, 2024 0 Comments InstagramThis 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 High-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (Posted: yesterday) A Depo-Provera lawsuit indicates that a Washington state woman must receive ongoing medical monitoring and brain scans due to a high-risk brain tumor allegedly caused by the birth control shot. MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Meningioma Lawyers Reappointed to MDL Leadership Roles (03/25/2026)Depo-Provera Brain Tumor Symptoms Reported Among Birth Control Users (03/19/2026)Depo Injection Lawsuit Claims Birth Control Shot Caused Meningioma Brain Tumor (03/17/2026) Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (Posted: 3 days ago) An Illinois woman has joined a growing number of plaintiffs alleging that the Medtronic Intellis neurostimulator, and similar devices, may fail to relieve chronic pain and instead lead to worsening complications. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro 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)Abbott, Boston Scientific Oppose Spinal Cord Stimulator Lawsuit MDL (03/20/2026) Court Outlines Plan To Prepare Suboxone Tooth Decay Lawsuits for Trial in Early 2028 (Posted: 4 days ago) Four Suboxone tooth decay lawsuits will eventually be selected and prepared for bellwether trials set to begin in March 2028, according to a court order. MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Film Lawsuit Filed by 46 Users Alleging Drug Makers Ignored Years of Dental Injury Reports (03/03/2026)100 Suboxone Film Tooth Decay Lawsuits Selected for Next Phase of Bellwether Discovery (02/13/2026)Problems With Suboxone Dental Injury Records Collection Continues in MDL (01/26/2026)
High-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (Posted: yesterday) A Depo-Provera lawsuit indicates that a Washington state woman must receive ongoing medical monitoring and brain scans due to a high-risk brain tumor allegedly caused by the birth control shot. MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Meningioma Lawyers Reappointed to MDL Leadership Roles (03/25/2026)Depo-Provera Brain Tumor Symptoms Reported Among Birth Control Users (03/19/2026)Depo Injection Lawsuit Claims Birth Control Shot Caused Meningioma Brain Tumor (03/17/2026)
Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (Posted: 3 days ago) An Illinois woman has joined a growing number of plaintiffs alleging that the Medtronic Intellis neurostimulator, and similar devices, may fail to relieve chronic pain and instead lead to worsening complications. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro 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)Abbott, Boston Scientific Oppose Spinal Cord Stimulator Lawsuit MDL (03/20/2026)
Court Outlines Plan To Prepare Suboxone Tooth Decay Lawsuits for Trial in Early 2028 (Posted: 4 days ago) Four Suboxone tooth decay lawsuits will eventually be selected and prepared for bellwether trials set to begin in March 2028, according to a court order. MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Film Lawsuit Filed by 46 Users Alleging Drug Makers Ignored Years of Dental Injury Reports (03/03/2026)100 Suboxone Film Tooth Decay Lawsuits Selected for Next Phase of Bellwether Discovery (02/13/2026)Problems With Suboxone Dental Injury Records Collection Continues in MDL (01/26/2026)