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.
More Window Blinds and Roman Shades Recalled Due to Strangulation Risk October 28, 2009 AboutLawsuits Add Your CommentsFollowing a recall of more than 5.4 million window shades and blinds in August, nearly one million more blinds and shades sold through Ikea, Bed Bath & Beyond and Hanover Direct/Domestications were recalled this week due to fears that their designs could result in children getting strangled.On Tuesday the U.S. Consumer Product Safety Commission announced the recall of 533,000 Ikea roller blinds, 364,000 Bed Bath & Beyond Roman shades, and 90,000 Hanover Direct Roman shades. The recalls come after at least three young children were nearly strangled to death by the shades.The Ikea recall includes all ISDANS, TUPPLUR and ENJE roller blinds, which have a looped bead chain which forms a free-standing loop that can wrap around a childโs neck if not secured to the wall or floor. The blinds are made of solid or sheer fabric with an orange warning label attached to the base of the blind marked with AA-136800-3. The blinds are 24 to 79 inches wide. The ENJE blinds have a glued label on the wall fitting with the Ikea logo, an article number, 5-digit supplier number, a date stamp and โMade in Taiwan.โ The blinds were sold at Ikea stores nationwide between July 2005 and July 2009.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 Bed Bath & Beyond recall includes the Dublin Energy Solution Roman Shades, which have exposed inner cords on the back which can get caught around a childโs neck. The shades were sold in navy, chocolate, khaki and cream colors and include a small orange, black and white warning label on the back of the head rail. The shades were sold at Bed Bath & Beyond stores nationwide and online from August 2007 through September 2009.The recall also includes Faux Suede Roman Shades from Hanover Direct, Inc., which is also known as Domestications. Like with the other Roman shades, the inner cord on the backside of shade is exposed and can get caught around a childโs neck. The shades have a style number of 12810A printed on the packaging box, and a sticker with the letters WS is on the head rail. The shades were sold in ivory, taupe, gold, plum wine red, midnight blue, moss green and dark brown. They were sold through catalog sales at online at www.domestications.com from January 2004 through December 2008.The U.S. CPSC and the manufacturers recommend that consumers immediately stop using these shades and blinds and contact the sellers for a free repair kit. Tags: Blinds, Ikea, Roman ShadesMore Lawsuit Stories Olympus Endoscope Lawsuit Filed Over ERCP Infection, Sepsis Linked to Contaminated Scope June 9, 2026 Dupixent Injection Lawsuits Consolidated in MDL Over CTCL Diagnoses June 9, 2026 Lawsuit Alleges Enfamil, Similac Cow’s Milk-Based Formula Caused Infant’s NEC Diagnosis June 9, 2026 0 Comments LinkedInThis 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 Olympus Endoscope Lawsuit Filed Over ERCP Infection, Sepsis Linked to Contaminated Scope (Posted: today)Lawsuit alleges Olympus failed to address known problems with sterilizing duodenoscopes, leading to a fatal ERCP infection years after federal regulators first raised concerns about the devices.MORE ABOUT: SCOPE INFECTION LAWSUITPediatric Sepsis Cases Contribute to More Than 1,800 Childrenโs Deaths Annually in U.S.: Study (03/31/2026)Infections After Colonoscopy, ERCP May Result in Lawsuits Over Olympus Scope Problems (03/27/2026) Boston Scientific Stimulator Lawsuits Centralized in Federal MDL (Posted: yesterday)Federal regulators have centralized at least 23 Boston Scientific spinal cord stimulator lawsuits in a multidistrict litigation that excludes multiple similar claims involving Abbott and Nevro implants.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (06/02/2026)Spinal Cord Stimulator Malpractice Lawsuit Claims Device Left Veteran Partially Paralyzed (05/29/2026)Abbott Spinal Cord Stimulator Problems Resulted in Severe Paralysis: Lawsuit (05/19/2026) Depo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims (Posted: 4 days ago)A Depo-Provera meningioma lawsuit indicates that a woman suffered permanent and debilitating injuries after needing to have a brain tumor surgically removed.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Caused Meningioma 29 Years After First Birth Control Shots: Lawsuit (05/22/2026)Depo-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)
Olympus Endoscope Lawsuit Filed Over ERCP Infection, Sepsis Linked to Contaminated Scope June 9, 2026
Olympus Endoscope Lawsuit Filed Over ERCP Infection, Sepsis Linked to Contaminated Scope (Posted: today)Lawsuit alleges Olympus failed to address known problems with sterilizing duodenoscopes, leading to a fatal ERCP infection years after federal regulators first raised concerns about the devices.MORE ABOUT: SCOPE INFECTION LAWSUITPediatric Sepsis Cases Contribute to More Than 1,800 Childrenโs Deaths Annually in U.S.: Study (03/31/2026)Infections After Colonoscopy, ERCP May Result in Lawsuits Over Olympus Scope Problems (03/27/2026)
Boston Scientific Stimulator Lawsuits Centralized in Federal MDL (Posted: yesterday)Federal regulators have centralized at least 23 Boston Scientific spinal cord stimulator lawsuits in a multidistrict litigation that excludes multiple similar claims involving Abbott and Nevro implants.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (06/02/2026)Spinal Cord Stimulator Malpractice Lawsuit Claims Device Left Veteran Partially Paralyzed (05/29/2026)Abbott Spinal Cord Stimulator Problems Resulted in Severe Paralysis: Lawsuit (05/19/2026)
Depo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims (Posted: 4 days ago)A Depo-Provera meningioma lawsuit indicates that a woman suffered permanent and debilitating injuries after needing to have a brain tumor surgically removed.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Caused Meningioma 29 Years After First Birth Control Shots: Lawsuit (05/22/2026)Depo-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)