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.
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.
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.
Sports Betting Addiction Lawsuit Sports betting addiction lawsuits are being investigated for college students and young adults who developed gambling problems after using apps like FanDuel and DraftKings, alleging that the platforms failed to warn about the addictive nature of their features and marketing practices.
Dollar Tree Halloween Lantern Recall: Risk of Fire and Burns October 29, 2010 Staff Writers Add Your CommentsAbout 682,000 Dollar Tree children’s Halloween lanterns have been recalled due to the risk that they may overheat and the cause fires or burns. The Dollar Tree Halloween lantern recall was announced on Thursday by the U.S. Consumer Product Safety Commission (CPSC) after Dollar Tree Stores, Inc. received a report of the bulb in the lantern overheating. There have been no injuries reported in connection with the defective children’s lanterns.The recall affects the Dollar Tree Pumpkin, Ghost and Skull Halloween Lanterns. They are about 6 1/2 inches tall and sold in orange, white and black. They have a model number of 954437-13096-003-1005, which can be found on the bottom of the lanterns.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 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 COMPENSATIONThe lanterns were imported from China by Greenbrier International Inc., of Chesapeake, Virginia, and sold at Dollar Tree, Dollar Bill$, Occasions, Deal$ and Dollar Tree Deal$ stores nationwide for about $1 from August 2010 through October 2010.This is the second time in just days that Dollar Tree has had to issue a recall due to children’s toys overheating. On October 19, there was a Dollar Tree projector flashlight recall after it was found that the batteries and bulbs of the toys, featuring superheroes from Marvel Comics, could overheat.The CPSC recommends that consumers who purchased the recalled Halloween lanterns take them away from children immediately, remove and properly discard the batteries and return the lanterns to the place of purchase for a full refund. Tags: Burn, Children, Children Toy Recall, FireMore Lawsuit Stories Omnipod Recall Impacts Another 7 Million Defective Pods That May Cause DKA, Hospitalization May 27, 2026 Group of 38 Hair Relaxer Cancer Lawyers Reappointed to MDL Leadership Roles May 27, 2026 Flavored Nitrous Oxide Lawsuit Alleges Amazon Canisters Caused Woman’s Death May 27, 2026 0 Comments 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 Omnipod Recall Impacts Another 7 Million Defective Pods That May Cause DKA, Hospitalization (Posted: today)Federal regulators have expanded an Omnipod recall after reports that internal tubing defects may cause insulin leaks and under-delivery, potentially triggering dangerous blood sugar spikes.MORE ABOUT: OMNIPOD RECALL LAWSUITRecalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (04/30/2026)Insulet OmniPod 5 Recall Lawsuits May Be Filed Over Problems Resulting in Diabetic Ketoacidosis, Hospitalization and Death (03/24/2026)Omnipod 5 Insulin Pump Recall Follows Reports of Serious Injuries: FDA (03/20/2026) GalaFLEX Mesh Problems May Lead Women To Require Breast Implant Removal Surgery (Posted: yesterday)Growing reports of GalaFLEX breast mesh complications have raised concerns about women who required explant surgery, revision procedures or implant removal after the synthetic mesh was used during breast augmentation, breast lift, implant revision or reconstruction surgery.MORE ABOUT: BREAST MESH LAWSUITGalaflex Breast Mesh Lawsuits Filed Against Becton Dickinson in Rhode Island (05/05/2026)Breast Mesh Implant Complications Often Leave Women Asking If They Have a Lawsuit (03/05/2026)Cosmetic Surgeons Warn Against Using Internal Bra Mesh for Breast Lifts (12/11/2025) Depo-Provera Caused Meningioma 29 Years After First Birth Control Shots: Lawsuit (Posted: 5 days ago)Pfizer continues to face Depo-Provera lawsuits from across the U.S., including one by a woman who says she learned of her brain tumor nearly 30 years after she stopped receiving the injections.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Lawsuit Filings Exceed 6,000, As Court Prepares for First Test Trials (05/18/2026)Intracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (05/12/2026)Lawsuit Blames Depo Shot for Brain Tumors, Intense Headaches (04/28/2026)
Omnipod Recall Impacts Another 7 Million Defective Pods That May Cause DKA, Hospitalization May 27, 2026
Omnipod Recall Impacts Another 7 Million Defective Pods That May Cause DKA, Hospitalization (Posted: today)Federal regulators have expanded an Omnipod recall after reports that internal tubing defects may cause insulin leaks and under-delivery, potentially triggering dangerous blood sugar spikes.MORE ABOUT: OMNIPOD RECALL LAWSUITRecalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (04/30/2026)Insulet OmniPod 5 Recall Lawsuits May Be Filed Over Problems Resulting in Diabetic Ketoacidosis, Hospitalization and Death (03/24/2026)Omnipod 5 Insulin Pump Recall Follows Reports of Serious Injuries: FDA (03/20/2026)
GalaFLEX Mesh Problems May Lead Women To Require Breast Implant Removal Surgery (Posted: yesterday)Growing reports of GalaFLEX breast mesh complications have raised concerns about women who required explant surgery, revision procedures or implant removal after the synthetic mesh was used during breast augmentation, breast lift, implant revision or reconstruction surgery.MORE ABOUT: BREAST MESH LAWSUITGalaflex Breast Mesh Lawsuits Filed Against Becton Dickinson in Rhode Island (05/05/2026)Breast Mesh Implant Complications Often Leave Women Asking If They Have a Lawsuit (03/05/2026)Cosmetic Surgeons Warn Against Using Internal Bra Mesh for Breast Lifts (12/11/2025)
Depo-Provera Caused Meningioma 29 Years After First Birth Control Shots: Lawsuit (Posted: 5 days ago)Pfizer continues to face Depo-Provera lawsuits from across the U.S., including one by a woman who says she learned of her brain tumor nearly 30 years after she stopped receiving the injections.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Lawsuit Filings Exceed 6,000, As Court Prepares for First Test Trials (05/18/2026)Intracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (05/12/2026)Lawsuit Blames Depo Shot for Brain Tumors, Intense Headaches (04/28/2026)