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 Proposes Lowering Maximum Levels Of Flouride Allowed In Bottled Water April 4, 2019 Martha Garcia Add Your CommentsFederal health regulators are proposing new rules that would lower the allowable levels of fluoride in bottled water.The FDA announced a proposed rule on April 2, citing the need to seek a balance between the benefits and risks to consumersโ teeth and health.In 2015, the U.S. Public Health Service (PHS) recommended the levels of fluoride added to community water systems be lowered to 0.7 mg/L. The proposed FDA regulation would lower the limit manufacturers are allowed to add to their bottled water products to match that same PHS level.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 COMPENSATIONThis rule only lowers the amount of fluoride in bottled water if it is added by manufacturers. It does not regulate the total amounts allowed overall, including any fluoride present in the water source.Fluoride is an important chemical that is added to water and other personal care products to help reduce cavities and tooth decay. However, too much fluoride over a long period of time or when the teeth are forming under the gums can cause dental fluorosis, or changes to the appearance of the tooth enamel. It can cause dark brown and yellow staining or damaged enamel.Extremely high levels of fluoride can cause fluoride toxicity, which leads to bone deformations, abdominal pain, nausea, seizures, vomiting, and muscle spasms.The FDA warned that it is important to find the balance between too little and too much fluoride. This is especially important for children under eight years old whose permanent teeth are still forming. Fluoride is important, but too much fluoride can harm their dental development.โItโs the FDAโs responsibility to ensure that if fluoride is added to bottled water, it is added at appropriate levels so that consumers receive its important health benefit while also being protected from potential adverse effects,โ Dr. Susan Mayne, director of FDAโs Center for Food Safety and Applied Nutrition, said in a press release. โBy lowering the allowable level of fluoride in bottled water following its addition by the manufacturer, we can help ensure that consumers enjoy the important health benefits of fluoride while preventing overexposure.โMost fluoride added to bottle water is at or below the limit being proposed by the FDA. Many manufactures took the step to lower added fluoride levels after the PHS proposed new limits in 2015. Many companies already adhere to the lower 0.7 mg/L level limit.The proposed fluoride rule will be open for public comment for 60 days. This allows the public, industry, and other parties to share comments regarding the proposed regulation with the FDA before the ruling is finalized. Written by: Martha GarciaHealth & Medical Research WriterMartha 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: Bottled Water, Children, FlourideMore Lawsuit Stories Bard PowerPort Infection Lawsuit Claims Catheter Fractures Harbored Bacteria November 3, 2026 Chlorpyrifos Pesticide Exposure Detected in Infants, Raising New Neurotoxicity Concerns November 3, 2026 Medtronic Insulin Pump Lawsuit Filed Over Recalled MiniMed 600 Series Device November 3, 2026 0 Comments CommentsThis 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 Bard PowerPort Infection Lawsuit Claims Catheter Fractures Harbored Bacteria (Posted: today)An Illinois man’s lawsuit accuses C.R. Bard of using a defective material in its PowerPort port catheter’s construction, causing him to suffer an infection and device failure.MORE ABOUT: BARD POWERPORT LAWSUITFourth Bard PowerPort Bellwether Case Set for Trial Dec. 1, as Third Gets Underway (10/14/2026)Judge Clears Bard PowerPort Lawsuit for Trial, Rejecting Motion for Summary Judgment (10/02/2026)Bard PowerPort Infection Lawsuit Set for Third Bellwether Trial to Begin Oct. 13 (09/14/2026) Abbott Sales Reps Kept Trying to Reprogram Failed SCS Implant: Lawsuit (Posted: yesterday)An Abbott SCS Implant lawsuit claims the manufacturers’ sales representatives potentially delayed removal of a failed device due to attempts to try to reprogram it.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Proclaim Elite Lawsuit Alleges Spinal Cord Stimulator Malfunction Worsened Chronic Pain (10/29/2026)Boston Scientific Spectra WaveWriter Lawsuit Alleges Lead Fracture, Migration and Painful Electric Shocks (10/21/2026)Abbott Spinal Cord Stimulator Lead Problems Caused Burning, Shocks, Lawsuit Alleges (10/16/2026) Ozempic Blindness Lawsuit Alleges Novo Nordisk Concealed NAION Risks (Posted: 4 days ago)A woman’s lawsuit accuses Novo Nordisk of ignoring and downplaying risks of vision loss linked to GLP-1 drugs like Ozempic.MORE ABOUT: OZEMPIC LAWSUITGLP-1 Vision Loss Lawsuit Alleges Ozempic Caused Man to Become Legally Blind (10/13/2026)Ozempic Injection Lawsuit Claims Diabetes Medication Caused Vision Loss (09/22/2026)Lawsuit Blames Mounjaro, Ozempic Side Effects for Vision Loss (09/15/2026)
Chlorpyrifos Pesticide Exposure Detected in Infants, Raising New Neurotoxicity Concerns November 3, 2026
Bard PowerPort Infection Lawsuit Claims Catheter Fractures Harbored Bacteria (Posted: today)An Illinois man’s lawsuit accuses C.R. Bard of using a defective material in its PowerPort port catheter’s construction, causing him to suffer an infection and device failure.MORE ABOUT: BARD POWERPORT LAWSUITFourth Bard PowerPort Bellwether Case Set for Trial Dec. 1, as Third Gets Underway (10/14/2026)Judge Clears Bard PowerPort Lawsuit for Trial, Rejecting Motion for Summary Judgment (10/02/2026)Bard PowerPort Infection Lawsuit Set for Third Bellwether Trial to Begin Oct. 13 (09/14/2026)
Abbott Sales Reps Kept Trying to Reprogram Failed SCS Implant: Lawsuit (Posted: yesterday)An Abbott SCS Implant lawsuit claims the manufacturers’ sales representatives potentially delayed removal of a failed device due to attempts to try to reprogram it.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Proclaim Elite Lawsuit Alleges Spinal Cord Stimulator Malfunction Worsened Chronic Pain (10/29/2026)Boston Scientific Spectra WaveWriter Lawsuit Alleges Lead Fracture, Migration and Painful Electric Shocks (10/21/2026)Abbott Spinal Cord Stimulator Lead Problems Caused Burning, Shocks, Lawsuit Alleges (10/16/2026)
Ozempic Blindness Lawsuit Alleges Novo Nordisk Concealed NAION Risks (Posted: 4 days ago)A woman’s lawsuit accuses Novo Nordisk of ignoring and downplaying risks of vision loss linked to GLP-1 drugs like Ozempic.MORE ABOUT: OZEMPIC LAWSUITGLP-1 Vision Loss Lawsuit Alleges Ozempic Caused Man to Become Legally Blind (10/13/2026)Ozempic Injection Lawsuit Claims Diabetes Medication Caused Vision Loss (09/22/2026)Lawsuit Blames Mounjaro, Ozempic Side Effects for Vision Loss (09/15/2026)