MDL Sought for Apple Lawsuits Over AirTag Stalking Problems and Damages Caused By Unauthorized Tracking
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 Parkinson’s Disease Lawsuit Chlorpyrifos lawsuits are being investigated for individuals diagnosed with Parkinson’s 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.
American Signature Entertainment Centers Recalled Due to Fall Hazard June 18, 2010 Staff Writers Add Your CommentsAbout 24,000 American Signature entertainment centers have been recalled over reports that several of them collapsed, sometimes falling onto consumers. The entertainment center recall was announced on June 16 by the U.S. Consumer Product Safety Commission (CPSC) after the manufacturer, American Signature Inc., received at least four reports of the shelf above the television collapsing. At least two people have been injured, including a child whose fingers were struck and an adult who received a mouth injury that required stitches. There were also minor property damage reports received as well.The CPSC has determined that the entertainment centers’ shelves can slip off and fall when the center is moved.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 recall affects about 24,000 American Signature, Inc. entertainment centers with the model names “Arts and Crafts,” Vineyard Manor,” “Lake Cottage,” “Studio One,” “West Indies,” and “Plantation Cove.” The entertainment centers were sold in the colors dark brown, natural, black and white and have fixed or adjustable shelves.The entertainment centers were sold at Value City Furniture, Rooms Today and American Signature Furniture stores nationwide from October 2002 through December 2009 for about $1,650.The CPSC recommends that consumers who have bought the recalled entertainment centers avoid moving them until they are repaired. American Signature Inc. has said it is sending a free repair kit to those who purchased the entertainment center. Consumers with questions can visit the company’s websites at www.vcf.com and www.asfurniture.com. Tags: Defective Product, Product RecallMore Lawsuit Stories Nearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials August 12, 2026 MDL Sought for Apple Lawsuits Over AirTag Stalking Problems and Damages Caused By Unauthorized Tracking August 12, 2026 Recalled LINX Device Caused Recurrence of GERD Symptoms, Requiring Surgical Removal: Lawsuit August 12, 2026 4 Comments Wendy August 7, 2021 I have the same one in dark wood .. Sad this has happened to this product. DM Hurley March 22, 2015 I am in Georgia. Where are you? M Jandris August 13, 2014 I have one exactly like the picture shown, in the same black, for sale…where are you located?? D M Hurley July 15, 2014 Please share with me the identity of the manufacturer of the Plantation Cove Entertainment Unit. I want one very badly. 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 Nearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (Posted: yesterday)C.R. Bard and its Becton Dickinson parent company face more than 3,700 Bard PowerPort lawsuits that claim the port catheters are defectively designed.MORE ABOUT: BARD POWERPORT LAWSUITBard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)New Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026)Bard PowerPort Fracture Lawsuit Set For Second Bellwether Trial in Aug. 2026 (05/29/2026) Dupixent CTCL Studies Highlighted Cancer Risks For Years, Lawsuit Alleges (Posted: 2 days ago)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: 3 days ago)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)
Nearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials August 12, 2026
MDL Sought for Apple Lawsuits Over AirTag Stalking Problems and Damages Caused By Unauthorized Tracking August 12, 2026
Recalled LINX Device Caused Recurrence of GERD Symptoms, Requiring Surgical Removal: Lawsuit August 12, 2026
Nearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (Posted: yesterday)C.R. Bard and its Becton Dickinson parent company face more than 3,700 Bard PowerPort lawsuits that claim the port catheters are defectively designed.MORE ABOUT: BARD POWERPORT LAWSUITBard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)New Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026)Bard PowerPort Fracture Lawsuit Set For Second Bellwether Trial in Aug. 2026 (05/29/2026)
Dupixent CTCL Studies Highlighted Cancer Risks For Years, Lawsuit Alleges (Posted: 2 days ago)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: 3 days ago)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)