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.
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
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.
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.
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.
Fosamax Fracture Lawsuit Remanded by MDL Judge December 1, 2009 AboutLawsuits Add Your CommentsThe judge who is presiding over the consolidated federal Fosamax litigation, which involves claims that Merck & Co. failed to warn that their osteoporosis drug may increase the risk of jaw necrosis, has ordered that one lawsuit filed by a plaintiff who alleges that she suffered hip and femur fractures from Fosamax side effects, should be removed from the multidistrict litigation (MDL), and return to the court where it was originally filed for further proceedings.Merck currently faces more than 900 Fosamax lawsuits filed by former users of their popular medication, who allege that the drug maker failed to adequately research the side effects of their product and warn about potential problems that could occur. The vast majority of the cases involve allegations that long-term use of Fosamax caused osteonecrosis of the jaw, or decay of the jaw bone. However, studies have suggested that Fosamax problems may also include a risk of femur fractures and issues with bone in the hips, shoulders and knees.On November 20, U.S. District Judge John F. Keenan ordered that Phyllis Molnarโs Fosamax fracture lawsuit be remanded back to the District of New Jersey, where it was originally filed. Molnar alleges in her lawsuit that Fosamax use caused her to fracture her hip and femur.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 COMPENSATIONA study published in the May/June 2008 issue of the Journal of Orthopedic Trauma found a Fosamax femur fracture pattern that was 98% specific to users of the osteoporosis drug, involving low-energy fractures that were typically caused by falls from a standing height or less. The study also found that the average duration of Fosamax use was longer among those who had signs of these specific femur fractures than those who did not.The U.S. Judicial Panel on Multidistrict Litigation consolidated all federal lawsuits over Fosamax jaw problems before Judge Keenan for coordinated pretrial proceedings in the U.S. District Court for the Southern District of New York. The first Fosamax trial in the MDL was in September, ending in a mistrial after jurors could not agree on a verdict. The second scheduled Fosamax jaw necrosis trial was dismissed by Judge Keenan last month, after he found that the plaintiff could not establish that Fosamax caused her jaw damage.Molnar filed to have her Fosamax fracture lawsuit removed from the MDL in September, saying that the leadership attorneys in the MDL were not openly sharing the documentation necessary to pursue her claim. The motion asked Judge Keenan to either force the release of documentation to Molnarโs attorneys, or allow the case to be remanded back to the District of New Jersey, where they will be able to pursue independent discovery. Attorneys for Merck sought to block the remand of the case, saying that the MDL was not limited to Fosamax ONJ lawsuits.In his ruling in favor of Molnarโs case being remanded, Judge Keenan stated that the evidence of general causation leading to femur and hip fractures would likely differ substantially from cases dealing with jaw bone damage. and justified remand. Tags: Fosamax, Fosamax Fracture, Hip Fracture, Jaw Necrosis, Osteonecrosis of the Hip, Osteonecrosis of the Jaw Image Credit: |More Fosamax Lawsuit Stories Fosamax Fracture Lawsuits Dismissed Again, After Judge Rules FDA Rejected Label Warning Change March 24, 2022 Zometa Side Effects Increase Risk of Osteonecrosis of the Jaw: Study January 14, 2021 Study Questions Whether Fosamax And Similar Bone Drugs Provide Benefits After Seven Years of Use December 10, 2020 2 Comments harriet March 23, 2010 i also had afosamax fracture my femur was shattered and today i have a rod in me still have trouble walking more than one block donna March 5, 2010 BOTH FEMURS have broken as described in these cases PhoneThis 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 Dupixent CTCL Studies Highlighted Cancer Risks For Years, Lawsuit Alleges (Posted: today)A Dupixent CTCL lawsuit indicates manufacturers have long known the eczema treatment was linked to an increased cancer risk, but failed to warn doctors or patients.MORE ABOUT: DUPIXENT LAWSUITCTCL Lawsuit Alleges Diagnosis Came After Less Than a Year of Dupixent Use (07/29/2026)Lawsuit Alleges Dupixent Caused Mycosis Fungoides Diagnosis (07/21/2026)Dupixent MDL Judge To Meet With Lawyers for Initial Case Management Conference in October 2026 (06/25/2026) Abbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims (Posted: yesterday)Manufacturer wants the Judicial Panel on Multidistrict Litigation to reject a proposal by a group of plaintiffs to consolidate all federal Abbott spinal cord stimulator lawsuits.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (08/06/2026)Spine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026)Spinal Cord Stimulator Reprogramming Caused Electric Shocks, Worsening Pain: Lawsuit (07/27/2026) AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis (Posted: 4 days ago)A Pennsylvania man has filed an AngioDynamics SmartPort lawsuit alleging catheter defects promoted bacterial growth, causing a severe infection and sepsis only weeks after implantation.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Sepsis Lawsuit Claims Defective SmartPort Implant Caused Infection (07/22/2026)SmartPort Catheter Lawsuit Claims Defective AngioDynamics Port-a-Cath Caused Infection (07/14/2026)Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (07/07/2026)
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