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.
Fitbit Ionic Recalls Impacts Nearly 1.7 Million Smartwatches Following Reports of Severe Burns, Injuries Fire and Burn HazardMore than 115 reports have been made of overheating batteries with 78 confirmed Fitbit burn injuries in the U.S. March 2, 2022 Randy Dixon, Jr. Add Your CommentsMore than a million Fitbit smartwatches are being recalled following dozens of reports involving burn injuries that occurred after the fitness tracker battery overheated.The Fitbit Ionic recall was announced today by the U.S. Consumer Product Safety Commission (CPSC), after the Google-owned company received at least 115 reports of problems with the lithium-ion battery overheating.At least 78 individuals in the U.S. have experienced Fitbit burn injuries from the Ionic Smartwatches, with 4 cases involving second-degree burns and 2 cases of third-degree burns.Available in brick and mortar stores like Best Buy, Target, and Kohlโs as well as online through Amazon.com and Fitbit.com, over 1 million Fitbit Ionic smartwatches have been sold in the U.S., with a retail price from $200 to $330. Close to another 700,000 of the recalled Fitbit watches were sold internationally between September 2017 and December 2021.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 COMPENSATIONThe recalled Ionic smartwatches were last produced by Fitbit in 2020, and were marketed as a GPS device, intended to track physical activity, heart rate, and sleep, as well as provide health and wellness insights.The Fitbit recall impacts Ionic Smartwatch with model numbers: Ionic FB503CPBU, Ionic FB503GYBK, Ionic FB503WTGY, and Ionic FB503WTNV. The model number can be found on the back of the device close to where the band attaches. The affected watches have a polyurethane band, a 1.4-inch color LCD screen, and were sold in slate blue/burnt orange, charcoal/smoke gray, blue gray/silver gray, and were also sold as an Adidas special edition in blue and silver gray. All have “Fitbit” printed on the front of the watch.No other Fitbit smartwatches or fitness trackers are being recalled at this time due to battery problems, and it is unclear what design choices are resulting in the Ionic burn injuries.Consumers who own a Fitbit Ionic Smartwatch are being cautioned to immediately stop the use of the device, and contact Fitbit to begin the return process. Fitbit will provide a pre-paid package for the return of all recalled Ionic Smartwatches. Once that package is received by Fitbit a refund of $299 will be issued. Participating consumers will also be provided a discount code for 40% off of select Fitbit devices.Consumers who have questions or wish to begin the return process can contact Fitbit toll-free by phone at 888-925-1764 or by visiting their website online. Tags: Burns, Fitbit, Smartwatch RecallMore Lawsuit Stories DraftKings Gambling Lawsuit Alleges Illegal Scheme Fueled Addiction October 27, 2026 Snapchat Child Sexual Abuse Lawsuit Alleges Predator Targeted 9-Year-Old Girl October 27, 2026 Olympus Scope Problems Lead to FDA Import Warning October 27, 2026 1 Comments Barbara February 2, 2025 I have a fitbit smartphone every time I wear it, it’s gets to hot on my arm so I stop wearing it 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 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 DraftKings Gambling Lawsuit Alleges Illegal Scheme Fueled Addiction (Posted: today)A Massachusetts man’s lawsuit claims he “lost everything” after DraftKings employees began illegally running bets for him across the state border to a casino where they worked.MORE ABOUT: SPORTS BETTING ADDICTION LAWSUITDraftKings Lawsuit Seeks Discovery Into Gambling Algorithms, Bonuses and VIP Rewards (10/22/2026)DraftKings AI Lawsuit Alleges Gambling Promotions Targeted Users Likely to Lose Money (10/07/2026)DraftKings ‘Free Bet’ Promos Targeted Problem Gamblers Using AI: Report (09/29/2026) Lawsuit Claims Defective Apple AirTag Safety Features Allowed Domestic Violence Stalking (Posted: yesterday)A womanโs lawsuit claims her abusive former partner concealed an Apple AirTag in their 10-year-old daughterโs shoe to monitor her location.MORE ABOUT: APPLE AIRTAG LAWSUITLawsuit Alleges Apple AirTag Tracker Used to Monitor Womanโs Location (10/14/2026)Apple AirTag Stalking Lawsuits Consolidated in Northern District of California (10/08/2026)Apple AirTag Lawsuit Filed After Tracking Device Found Hidden Under Womanโs Car (09/24/2026) Parietene Hernia Mesh Lawsuit Alleges Defective Covidien Implant Caused Severe Nerve Damage, Chronic Pain (Posted: 4 days ago)Covidien faces a hernia mesh lawsuit from a man who says he suffered nerve damage and other injuries after the product failed, requiring removal surgery.MORE ABOUT: HERNIA MESH LAWSUITBard Ventralex Hernia Mesh Failure Lawsuit Alleges Implant Design Led to Infection (10/15/2026)Covidien ProGrip Mesh Lawsuit Scheduled for March 2027 Jury Trial (10/06/2026)Judge Sets Next Covidien Hernia Mesh Lawsuit for Trial in January 2027 (09/11/2026)
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