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.
Chlorpyrifos Parkinsonโs Disease Lawsuit Chlorpyrifos lawsuits are being investigated for individuals diagnosed with Parkinsonโs disease after direct, residential, occupational or Gulf War pesticide exposure.
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.
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.
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.
FDA Seeks To Address Concerns Over Toxic Metals In Baby Food March 15, 2021 Russell Maas Add Your CommentsIn the wake of a recent Congressional report that highlighted dangerous levels of toxic heavy metals in many popular baby foods, federal health officials are preparing to launch a series of regulatory actions, aimed at setting action levels for certain contaminants, as well as increasing facility inspections and product sampling.The FDA issued a statement on March 5, announcing new initiatives aimed at reducing harmful chemicals from entering or developing in baby food products, as well as boosting compliance and enforcement actions.The initiatives outlined in the release include a near term commitment to review the current action levels for contaminants in baby foods, and to continuously monitor those levels and lower them if appropriate. Determinations made from the review of action levels for contaminants will be provided to the industry with guidance on how to meet new obligations.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 COMPENSATIONUnder the plan, the FDA will begin working with government, academia, and stakeholders of the food industry to review and develop research to determine the allowable levels of harmful chemicals such as lead, arsenic, cadmium and mercury in baby food products.The FDA also announced it will begin increasing inspections of food manufacturing facilities while boosting sampling and testing of foods for babies and young children. These tests and results will be made available to the public, according to the agency.In addition to the initiatives outlined in the release, the FDA also issued a letter to baby and children food manufacturers on March 5, reminding them of their legal responsibility to ensure the safety of their products under the Federal Food, Drug, and Cosmetic Act. The letter reiterated that manufacturers have an existing responsibility to consider risks from chemical hazards which include toxic elements levels on final products.โOur new activities will further efforts that the agency has continued to take in this area, including our work in 2020 to finalize an action level for inorganic arsenic in infant rice cereal. Weโll be working to develop additional action levels, finalize our draft guidance on reducing inorganic arsenic in apple juice and publish a draft guidance that will establish action levels for lead in juices,โ the FDA statement, attributed to acting commissioner of Food and Drugs, Janet Woodcock, and Susan T. Mayne, director of the Center for Food Safety and Applied Nutrition, states. โThese activities, along with an increase in sampling and reporting, will help continue to drive down levels of toxic elements in foods.โThe initiatives were announced on the heels of a House Oversight Committee report released on February 4, which highlighted internal documents and testing data indicating baby food products manufactured by Gerber (d/b/a Nestlรฉ Nutrition), Beech-Nut Nutrition, Plum and others contain dangerous levels of heavy metals, which are toxic to infants and may result in permanent neurological damage.Findings from the U.S. Congressional report indicated some baby foods contain more than 91 times the maximum level of arsenic allowed in bottled water; 177 times the allowable levels of lead, 69 times the limits on cadmium, and five times the levels of allowable mercury.As a result of the reportโs findings, a growing number of baby food lawsuits continue to be filed throughout the federal court system nationwide. Many of the complaints against the baby food manufacturers raise common allegations that the products were falsely advertised as safe for children, while containing harmful levels lead, arsenic, cadmium and mercury.The FDA and U.S. Centers for Disease Control and Prevention (CDC) have long maintained exposing infants and children to toxic heavy metals can cause a permanent decrease in IQ, an increased risk of future criminal and antisocial behavior, and untreatable and frequently permanent brain damage.Heavy metal exposure to infants is a serious concern.ย Lead exposure at any level is extremely unsafeย for children. Prior studies have linked heavy metal exposure toย behavioral impairments, brain damage, damage to the nervous system, seizures, growth impairments, and even death. More oversight is needed to help protect infants from serious health side effect sand long-term health damage, the congressional report concluded. Written by: Russell MaasManaging Editor & Senior Legal JournalistRussell Maas is a paralegal and the Managing Editor of AboutLawsuits.com, where he has reported on mass tort litigation, medical recalls, and consumer safety issues since 2010. He brings legal experience from one of the nationโs leading personal injury law firms and oversees the siteโs editorial strategy, including SEO and content development. Tags: Arsenic, Baby Food, Congress, Heavy Metals, ToxicityMore Baby Food Lawsuit Stories Court Excludes Expert Witnesses Linking Metal in Baby Foods to Autism, ADHD Among Children March 4, 2026 Tainted Baby Food Lawsuit Against Whole Foods, Hain Celestial Returned to Texas State Court February 27, 2026 Lead Exposure in Childhood May Increase Adolescent Depression: Study February 17, 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 Judge Sets Next Covidien Hernia Mesh Lawsuit for Trial in January 2027 (Posted: today)The U.S. District Judge presiding over all Covidien hernia mesh lawsuits has scheduled the next bellwether trial to begin on January 11.MORE ABOUT: HERNIA MESH LAWSUITCovidien Mesh Lawyers to Meet With MDL Judge This Week, Following Landmark Verdict (08/17/2026)Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (08/05/2026)Hernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026) Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit (Posted: yesterday)A South Carolina woman alleges an Abbott spinal cord stimulator malfunction caused painful electrical shocks that required removal surgery less than two years after implantation.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (09/04/2026)Judge Allows Back Stimulator Lawsuits Against Boston Scientific to Be Directly Filed in MDL (08/31/2026)Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (08/26/2026) Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (Posted: 2 days ago)The second Bard PowerPort lawsuit bellwether trial has ended in a $40 million verdict for the plaintiff who had the implant removed after the catheter broke and traveled to her heart.MORE ABOUT: BARD POWERPORT LAWSUITNearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026)Bard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)New Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026)
Court Excludes Expert Witnesses Linking Metal in Baby Foods to Autism, ADHD Among Children March 4, 2026
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Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit (Posted: yesterday)A South Carolina woman alleges an Abbott spinal cord stimulator malfunction caused painful electrical shocks that required removal surgery less than two years after implantation.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (09/04/2026)Judge Allows Back Stimulator Lawsuits Against Boston Scientific to Be Directly Filed in MDL (08/31/2026)Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (08/26/2026)
Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (Posted: 2 days ago)The second Bard PowerPort lawsuit bellwether trial has ended in a $40 million verdict for the plaintiff who had the implant removed after the catheter broke and traveled to her heart.MORE ABOUT: BARD POWERPORT LAWSUITNearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026)Bard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)New Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026)