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 Abbott and Nevro Spinal Cord Stimulator Lawsuits Centralized in New Federal MDLs October 5, 2026 GERD Implant Lawsuit Alleges Defective LINX Failed After Surgery October 5, 2026 Roundup Cancer Lawsuit Trial Underway in Missouri Court October 5, 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 NameThis 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 Abbott and Nevro Spinal Cord Stimulator Lawsuits Centralized in New Federal MDLs (Posted: yesterday)Federally filed lawsuits against Abbott Laboratories and Nevro over alleged spinal cord stimulator injuries have been consolidated into two separate multidistrict litigations in California and Illinois.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITSpinal Cord Stimulator Lawsuit Alleges Boston Scientific Device Failure Required Removal Surgery (09/29/2026)Nevro SCS Implant Lawsuit Alleges Sales Rep Programming Led to Permanent Nerve Damage (09/21/2026)Boston Scientific Spine Stimulator Lawsuit Filed Over Numbness, Incontinence, Erectile Dysfunction (09/16/2026) Judge Clears Bard PowerPort Lawsuit for Trial, Rejecting Motion for Summary Judgment (Posted: 4 days ago)A U.S. District Judge refused to dismiss a Bard PowerPort lawsuit just two weeks before it is supposed to go to trial, saying the manufacturer will have to convince a jury with their arguments and not him.MORE ABOUT: BARD POWERPORT LAWSUITBard PowerPort Infection Lawsuit Set for Third Bellwether Trial to Begin Oct. 13 (09/14/2026)Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (09/09/2026)Nearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026) Dupixent Lawyers Seek Leadership Positions in MDL Over Cancer Risks (Posted: 5 days ago)Plaintiffs propose that about a dozen attorneys be appointed to leadership positions in the growing Dupixent cancer litigation.MORE ABOUT: DUPIXENT LAWSUITDupixent Side Effects Lawsuit Alleges Drug Caused Cutaneous T-Cell Lymphoma (09/24/2026)Dupixent Side Effects Caused CTCL, Tumors, Lawsuit Alleges (09/10/2026)Dupixent Lymphoma Lawsuit Alleges Atopic Dermatitis Drug Led to Mycosis Fungoides Diagnosis (08/20/2026)
Abbott and Nevro Spinal Cord Stimulator Lawsuits Centralized in New Federal MDLs (Posted: yesterday)Federally filed lawsuits against Abbott Laboratories and Nevro over alleged spinal cord stimulator injuries have been consolidated into two separate multidistrict litigations in California and Illinois.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITSpinal Cord Stimulator Lawsuit Alleges Boston Scientific Device Failure Required Removal Surgery (09/29/2026)Nevro SCS Implant Lawsuit Alleges Sales Rep Programming Led to Permanent Nerve Damage (09/21/2026)Boston Scientific Spine Stimulator Lawsuit Filed Over Numbness, Incontinence, Erectile Dysfunction (09/16/2026)
Judge Clears Bard PowerPort Lawsuit for Trial, Rejecting Motion for Summary Judgment (Posted: 4 days ago)A U.S. District Judge refused to dismiss a Bard PowerPort lawsuit just two weeks before it is supposed to go to trial, saying the manufacturer will have to convince a jury with their arguments and not him.MORE ABOUT: BARD POWERPORT LAWSUITBard PowerPort Infection Lawsuit Set for Third Bellwether Trial to Begin Oct. 13 (09/14/2026)Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (09/09/2026)Nearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026)
Dupixent Lawyers Seek Leadership Positions in MDL Over Cancer Risks (Posted: 5 days ago)Plaintiffs propose that about a dozen attorneys be appointed to leadership positions in the growing Dupixent cancer litigation.MORE ABOUT: DUPIXENT LAWSUITDupixent Side Effects Lawsuit Alleges Drug Caused Cutaneous T-Cell Lymphoma (09/24/2026)Dupixent Side Effects Caused CTCL, Tumors, Lawsuit Alleges (09/10/2026)Dupixent Lymphoma Lawsuit Alleges Atopic Dermatitis Drug Led to Mycosis Fungoides Diagnosis (08/20/2026)