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.
Infant Inclined Sleeper Problems Result in Additional Recalls and Another Death August 1, 2019 Russell Maas Add Your CommentsFollowing yet another infant death linked to problems with inclined sleepers sold by a number of different companies, Dorel is the latest manufacturer to issue a recall for certain products sold under the Eddie Bauer and Disney labels, due to a risk that infants may roll over and become entrapped or suffocate.The U.S. Consumer Product Safety Commission (CPSC) announced an Eddie Bauer and Disney bassinet recall on July 31, because they may pose a roll over entrapment hazard, or a chin-to-chest airway blockage. The recalls come after yet another child death involving a similar product.Inclining infant sleepers and bassinets are designed to elevate the babyโs head and torso. Inclining the infant during sleep has been shown to help prevent acid-reflux or congestion. However, the design has proven to be potentially deadly after babies are old enough to rollover on their own, or if the incline of the bassinet forces the childโs chin down to his or her neck, creating an airway blockage.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 COMPENSATIONApproximately 24,000 of the Eddie Bauer Slumber and Soothe Bassinets with model number BT055CSY and the Disney Baby Doze and Dream Bassinet with model number BT071DHS are impacted by the recall. The inclined sleepers are either purple or beige in color and rectangular shaped with a soft bottom, cushioned fabric, and measure approximately two feet high. Customer may locate the model numbers on a label underneath of the inclined sleeper.The products were manufactured in China by Dorel China, and imported by Dorel Juvenile Group USA, of Foxboro, Massachusetts. They were distributed for sale at Target, Kmart, Ross, Marshalls, TJ Maxx and juvenile product stores nationwide from November 2014 through February 2017 for about $60.Customers are being asked to stop using the inclined bassinets immediately and to contact Dorel at 877-657-9546 or email them at inclinesleeperrecall@djgusa.com for information on how to receive a refund in the form of a $60 voucher.Inclined Sleeper Safety RisksInclined infant sleeper safety concerns were disclosed to the public in April 2019, when the CPSC issued a Fisher-Price Rockโn Play warning, instructing consumers to stop placing their infants in the sleepers by three months old, or before they begin to show signs that they can roll over independently. The warning was issued after the CPSC publicly recognized at least 32 infant deaths related to the products.Since the warning, several manufacturers issued recalls of inclined sleeper products in April including Fisher-Priceโs recall of 4.7 million Rockโn Play Sleepers and a recall of 694,000 Kids II inclined rocking sleepers. Fischer-Price subsequently released an additional inclined sleeper recall in June, impacting 71,000 inclined sleeping accessories sold with their Ultra-Lite Day & Night Play Yards.Fischer-Price has been riddled with a number of inclined sleeper individual wrongful death lawsuits and also a class action lawsuit alleging the manufacturer knew or should have known about the risk of problems, yet delayed announcing a recall or warning, and knowingly allowed parents to continue purchasing life threatening sleeper devices.One of the latest fatalities to be reported involved a 3-month old from Sinking Springs, Pennsylvania who suffocated while lying on his back in a hammock shaped Chicco USA Lullaby Dream Playard sleeper. According to Consumer Reports, the lawsuit filed against the manufacturer this month indicates the child suffocated due to his head being forced downward to his chin because of the sleeperโs incline, causing an airway blockage. Written by: Russell MaasManaging Editor & Senior Legal JournalistRussell Maas is a paralegal and the Managing Editor of AboutLawsuits.com, where he has reported on mass tort litigation, medical recalls, and consumer safety issues since 2010. He brings legal experience from one of the nationโs leading personal injury law firms and oversees the siteโs editorial strategy, including SEO and content development. Tags: Child Death, Childrens Furniture Recall, Class Action Lawsuit, Disney, Dorel, Eddie Bauer, Fisher-Price, Infant Deaths, Infant Furniture, Mattel, SuffocationMore Lawsuit Stories Jury Selection Underway in First Bard PowerPort Trial Over Infection Claims April 16, 2026 HeartMate II Wrongful Death Lawsuit Claims LVAD Implant Caused Thrombosis April 16, 2026 Video Game Addiction Lawsuit Claims Devs Use Behavioral Manipulation on Kids April 16, 2026 0 Comments FacebookThis 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 Jury Selection Underway in First Bard PowerPort Trial Over Infection Claims (Posted: yesterday)The first Bard PowerPort lawsuit bellwether trial commences next week involving claims that a man suffered a severe infection due to the port catheter’s allegedly defective design.MORE ABOUT: BARD POWERPORT LAWSUITJudge Blocks Juries From Hearing About IVC Filter Problems in Bard PowerPort Trials (04/08/2026)Port-a-Cath Lawsuit Alleges Power P.A.C. Break Down Resulted in Serious Port Catheter Infection (03/31/2026)Final Pretrial Conference in Bard PowerPort Lawsuit To Be Held April 9 (03/27/2026) Hearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (Posted: 2 days ago)A federal judge has scheduled general causation hearings for Depo-Provera brain tumor lawsuits for June 24 through 26.MORE ABOUT: DEPO-PROVERA LAWSUITHigh-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (04/06/2026)Depo-Provera Meningioma Lawyers Reappointed to MDL Leadership Roles (03/25/2026)Depo-Provera Brain Tumor Symptoms Reported Among Birth Control Users (03/19/2026) WaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (Posted: 3 days ago)A Louisiana man’s Boston Scientific WaveWriter Alpha SCS lawsuit claims the implant failed to provide the promised pain relief and, in fact, made things worse before it needed to be surgically removed.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Neuromodulation Lawsuit Claims Spinal Cord Stimulator Exacerbated Chronic Pain (04/08/2026)Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (04/03/2026)Nevro Spinal Cord Stimulator Lawsuits Filed Over Device Malfunction, Failure (03/30/2026)
Jury Selection Underway in First Bard PowerPort Trial Over Infection Claims (Posted: yesterday)The first Bard PowerPort lawsuit bellwether trial commences next week involving claims that a man suffered a severe infection due to the port catheter’s allegedly defective design.MORE ABOUT: BARD POWERPORT LAWSUITJudge Blocks Juries From Hearing About IVC Filter Problems in Bard PowerPort Trials (04/08/2026)Port-a-Cath Lawsuit Alleges Power P.A.C. Break Down Resulted in Serious Port Catheter Infection (03/31/2026)Final Pretrial Conference in Bard PowerPort Lawsuit To Be Held April 9 (03/27/2026)
Hearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (Posted: 2 days ago)A federal judge has scheduled general causation hearings for Depo-Provera brain tumor lawsuits for June 24 through 26.MORE ABOUT: DEPO-PROVERA LAWSUITHigh-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (04/06/2026)Depo-Provera Meningioma Lawyers Reappointed to MDL Leadership Roles (03/25/2026)Depo-Provera Brain Tumor Symptoms Reported Among Birth Control Users (03/19/2026)
WaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (Posted: 3 days ago)A Louisiana man’s Boston Scientific WaveWriter Alpha SCS lawsuit claims the implant failed to provide the promised pain relief and, in fact, made things worse before it needed to be surgically removed.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Neuromodulation Lawsuit Claims Spinal Cord Stimulator Exacerbated Chronic Pain (04/08/2026)Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (04/03/2026)Nevro Spinal Cord Stimulator Lawsuits Filed Over Device Malfunction, Failure (03/30/2026)