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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.
Baby Shark Bath Toys Recalled Following Child Impalement, Laceration Injury ReportsThe top fins of the sharks have been linked to a dozen child injuries, some of which have led to hospitalizations June 23, 2023 Katherine McDaniel Add Your CommentsMore than seven million Baby Shark bath toys have been recalled, following reports of children suffering severe impalement and laceration injuries while using the toys, including incidents where children required medical attention or stitches.The U.S. Consumer Product Safety Commission (CPSC) announced the Zuru Baby Shark and Mini Baby Shark bath toy recall on June 22, warning the water activated child bath toys can cause serious injuries to children when they are used in a bath tub or shallow wading pool.Parents are being warned to immediately stop using the childrenโs bath toys and contact the manufacturer for a full refund.According to the recall, consumers have submitted at least 12 reports of children sustaining impalement injuries, lacerations, and puncture wounds to their genital, anorectal and facial areas after sitting on top of, or slipping and falling on top of, the sharkโs top fin. At least nine of the reported child injuries were severe and required medical attention or stitches to treat.Officials warn the top shark fins are hard enough to pierce a childโs skin and can result in deep cuts and puncture wounds. The child shark toys swim and sing once placed in water, and are especially dangerous when used in a shallow water setting, such as a bathtub or shallow wading pool, where a child can stand and potentially sit on top of the sharp shark fin or slip and fall on top of the fin and impale themselves.The recall impacts approximately 6.5 million full-size Robo Alive Junior Baby Shark Sing & Swim bath toys and approximately one million Mini Baby Shark Swimming bath toys.While only the full-size Baby Shark bath toys have been linked to the reported child injuries, the mini Baby Shark toys have also been recalled out of an abundance of caution, as they were also designed with a hard top fin.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 full-size Baby Shark bath toys measure seven inches in length, have a grooved top fin, and can be identified with model number 25282 printed on the bottom, along with a product date code that ranges from DG20190501 to DG20220619. They were sold individually, as well as in packs of three in the colors yellow, blue and pink from May 2019 until March 2023, and retailed between $13 and $15.The mini Baby Shark bath toys measure 4 inches in length, have a solid plastic top fin, and can be identified with model numbers 7163, 7175, 1766, or 25291 printed on the bottom, along with a product date code that ranges from DG2020615 to DG2023525. They were sold individually, in multi-packs, and as part of a Baby Shark Music Water Park playset in the colors yellow, blue, and pink from July 2020 until June 2020, and retailed from $6 to $20.The CPSC recommends consumers disable the tail fin of the toy by either cutting the fin off the full-sized shark toy or bending the fin of the mini shark toy, write the word โrecalledโ on the body of the shark, and visit Zuruโs website at https://www.recallrtr.com/bathshark to register the recalled toys. Once registered, they can then submit their unique recall code, along with a photo of their disabled and marked product. Zuru will provide consumers with a refund on a prepaid virtual MasterCard in the amount of $14 for a full-size shark or $6 for a mini shark toy.For more information, consumers may contact Zuru toll-free at 833-820-0839 from 8 a.m. to 7 p.m. on weekdays, or visit their website at https://www.recallrtr.com/bathshark or www.Zurutoys.com. Tags: Child Injury, Childrens Toy, Childrens Toy Recall, Impalement, LacerationMore Lawsuit Stories Robinhood Class Action Lawsuit Alleges Platformโs โEvent Contractsโ Violate Sports Betting Statutes June 15, 2026 Lawsuit Alleges Farberware 7-in-1 Pressure Cooker From Walmart Exploded, Caused Partial Thickness Burns June 15, 2026 Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect June 12, 2026 0 Comments CompanyThis 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 Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (Posted: 3 days ago)A spinal cord stimulator lawsuit claims that the Abbott Proclaim XR 5 system failed to treat a manโs chronic pain, instead leaving him with shocks and burning sensations.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026)Lawsuit 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) Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (Posted: 4 days ago)A Suboxone dental erosion lawsuit filed by nine plaintiffs accuses the manufacturer of knowing the film strips caused severe tooth decay and other oral health problems, but failed to warn the medical community or patients.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (05/20/2026)Lawsuit Alleges Suboxone Dental Damage Warnings Were Issued Too Late (05/07/2026)Study Finds No Birth Defect Risks From Suboxone When Compared to Methadone (04/30/2026) Covidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications (Posted: 5 days ago)A Covidien hernia mesh lawsuit will go before a jury next month after a federal judge rejected the manufacturer’s motion to have the case dismissed.MORE ABOUT: HERNIA MESH LAWSUITBard Ventralight Lawsuit Claims Hernia Mesh Failure Resulted in Ongoing Physical Disabilities (06/03/2026)Bard Ventralex Patch Lawsuit Claims Umbilical Hernia Mesh Failed, Requiring Removal Surgery (05/21/2026)Covidien ProGrip Mesh Complications Lawsuit Filed Over Alleged Defects and Failure To Warn Patients (04/21/2026)
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