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.
Stopping Zometa Use After Three Years Lowers Risk of Fracture: Study December 12, 2014 Irvin Jackson Add Your CommentsWhile use of Zometa and other bisphosphonate medications have been linked to an increased risk of bone fractures, new research suggests that stopping use of Zometa after three years may significantly reduce the risk.ย Zometa (zoledronic acid) is bisphosphonate injection used to reduce bone complications associated with multiple myeloma and bone metastases from solid tumors.Although it is part of a class of medications used to strengthen bones, side effects of Zometa and other related drugs have been linked to a risk of atypical femur fractures and deterioration of the jaw bone.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 COMPENSATIONIn a study published in this month’s issue of the Journal of Clinical Endocrinology & Metabolism, researchers found that patients taken off Zometa after three years had less risk of bone fractures. The study suggests that individuals could be kept off the drug for up to three years without seeing a significant risk of osteoporosis.Researchers looked at data on 1,233 women who received either Zometa injections or a placebo, finding that almost 55% of women who qualify as low risk and have no recent incident of risk fracture saw lower risk of suffering a bone fracture in the future if Zometa treatment was discontinued after three years.Concerns about the link between bone fractures and popular bisphophonate medications used for treatment and prevention of osteoporosis, such as Fosamax, Actonel, Boniva and others, led the FDA to issue recommendations in 2012 that patients limit use of the osteoporosis drugs to a three to five year period.A study by researchers from Loyola University Health System published in January recommended bisphosphonate medication users take a โdrug holidayโ, or a break from using the drug, to lessen the risk of femur fractures and other bone problems.In November 2013, researchers published a study in the medical journal Calcified Tissue International, which indicated that the increased risk of bone fractures with Zometaย and other osteoporosis drugs may have a genetic factor to explain why some users experience these atypical breaks in circumstances that would not normally cause a femur fracture.Several hundred product liability lawsuits have been filed against Novartis that allege the drug maker failed to adequately warn about the side effects of Zometa, as well as the similar injectable bisphosphonate Aredia.Fosamax is one of the most widely used bisphophonates, which is an oral medication prescribed to millions of Americans. In recent years, Merck has also faced a number of Fosamax fracture lawsuits that allege the drug maker failed to provide adequate warnings about the risks associated with the drug. Written by: Irvin JacksonSenior Legal Journalist & Contributing EditorIrvin Jackson is a senior investigative reporter at AboutLawsuits.com with more than 30 years of experience covering mass tort litigation, environmental policy, and consumer safety. He previously served as Associate Editor at Inside the EPA and contributes original reporting on product liability lawsuits, regulatory failures, and nationwide litigation trends. Tags: Aredia, Bisphosphonates, Fosamax, Osteoporosis, ZometaMore Lawsuit Stories Judge Clears Bard PowerPort Lawsuit for Trial, Rejecting Motion for Summary Judgment October 2, 2026 Paraquat Settlement Offers Rejected by Hundreds of Parkinsonโs Disease Plaintiffs October 2, 2026 Walmart Expert Grill Brush Recall Impacts 4.4 Million Over Wire Bristle Ingestion Risk October 2, 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 Judge Clears Bard PowerPort Lawsuit for Trial, Rejecting Motion for Summary Judgment (Posted: 2 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: 3 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) Lawyers Preparing 35 Suboxone Tooth Decay Lawsuits in Core Discovery Pool (Posted: 4 days ago)Nearly three dozen Suboxone tooth decay lawsuits are being prepared for early test trials, involving the deposition of plaintiffs who say they suffered tooth loss as a result of using the opioid addiction treatment.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Manufacturer Faces Nearly 18,000 Dental Erosion Lawsuits (07/09/2026)Suboxone Dry Mouth Lawsuit Claims Dental Problems Could Have Been Avoided With Sublocade Shot (06/18/2026)Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (06/11/2026)
Walmart Expert Grill Brush Recall Impacts 4.4 Million Over Wire Bristle Ingestion Risk October 2, 2026
Judge Clears Bard PowerPort Lawsuit for Trial, Rejecting Motion for Summary Judgment (Posted: 2 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)
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