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.
Spa Factory Aromatherapy Recall: Risk of Explosion For Children’s Fantasy Spa Fountains January 30, 2009 AboutLawsuits Add Your CommentsOver half a million Spa Factory Aromatherapy Fountain and Bath Benefits kits have been recalled by JAKKS Pacific Inc. and the U.S. Consumer Product Safety Commission (CPSC) after reports of young children suffering injuries caused by projectiles from exploding jars.The Spa Factory recall applies to fantasy fountains and kits sold between August 2008 and January 2009 at Sam’s Clubs, Wal-Marts, Targets and other toy stores throughout the United States.The products are marketed as a spa treatment for young girls, containing small jars with purple caps that are used to make Bath Bombs/Balls and Bath Fizzies.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 COMPENSATIONPressure from the buildup of carbon dioxide in the jars can cause the purple cap to blow off, potentially causing injury to the face. Citric acid contained in the jars may also get into the eyes, causing potential eye irritation.At least 88 reports have been received by the manufacturer of Spa Factory jars exploding, including 19 reports of injury. At least 13 of the reports of injury involve young children between 6 and 11 years old, who suffered welts, cuts, eye irritation and eye injuries from flying caps.The products recalled include the following models with an item number located on the bottom of the product packaging:Spa Factory Bath Benefits Kit 37836Spa Factory Deluxe Spa Fantasy Aromatherapy Fountain 37908Spa Factory Spa Fantasy Aromatherapy Fountain 37837Spa Factory Spa Fantasy Aromatherapy Fountain 54892Spa Factory Spa Fantasy Aromatherapy Fountain 54857In a notice posted on their the myspafactory.com website, JAKKS Pacific indicates that they have found that placing two small holes in the caps allows built up pressure to escape, eliminating the risk that the cap may explode off the jar.All Spa Factory Fantasy Aromatherapy Fountains and Bath Benefits kits sold after November 2008 contain caps with the two vent holes, and for those who have the original caps, free replacements are being provided free of charge by sending an email to caps@jakks.net. Tags: Childrens Toy, Fantasy Spa, Spa Factory Image Credit: |More Lawsuit Stories Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect June 12, 2026 Xcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis June 12, 2026 Rezurock Lawsuit Claims GVHD Medication Caused Debilitating Skin Condition, Prurigo Nodularis June 12, 2026 7 Comments Ana November 26, 2011 Wow…… i wanted this a few years ago for christmas but my mom decided to buy me a bracelet instead THANK GOD!!!!! now i started searching for it again and found this out i was really lucky i cant even imagine what would happen if my mom did buy it. Brittany July 23, 2010 I bought this set in like December 09 with the numbers Listed that were recalled and just saw the recall today and checked my daughters and it has no holes! Please explain to me why the sets that have. He issues were still being sold over a year later? This makes no sense to me! Christie January 1, 2010 What they fail to tell you is that not all of the item numbers were recalled, therefore they are still being sold. Both my daughter and niece received one for Christmas and last night, my niece’s exploded on her. It was on the walls, all over her face, her eyes and now her hands feel numb all the time. I checked my daughters box and her item number is not listed but does not have holes in the lids. It says to use by August 2010, which leads to me believe it was probably manufactured around August 2008. I think this product should have been recalled according to the product itself and not item numbers. The CPSC site lists 4 different item numbers for the same product. I think they only recalled those numbers that had complaints related to them but common sense would tell you that since the lids were the issue, they all need to replaced. What sense does it make to continue to sell the same product with the same faults just because no one happened to have issues with it yet? This sounds like the company was trying to avoid loss of profit by removing those boxes from the shelf and placed additional children at risk. This sounds like willful noncompliance to me. lexi January 1, 2010 i just bought one of those spa fantasy aromatherapy fountain yesterday,and today my aunt came over so i asked her if she wanted me to make a bath fizz balls and she said,”ya go ahead”, so i did when i was done i took it to her and i went to pick up a game that i played earlier and the were in the kitchen and all of a sudden we heared a big boomb,and what happend was the fizz ball exploed all ove the walls,celling,floor and my aunt, who is pregnant and could of gotten hert real baddly and we think she is so i just told them ” i will never let anyone in my family or just people i know,or friends and thier family’s buy and product from your company ever again. ” genesis l. July 19, 2009 i was going to buy a spa factory for my b-bay . i yust want to know when they will fix it?:-( Cherie June 6, 2009 This is a very dangerous product, It did explode all over my daughter in her face and eyes. So all you can say is let us know and you will replace the caps. How did this ever get onto shelves to sell to children to begin with if this could happen. I do not believe replacement caps with holes in them is going to satisfy parents of children that this has happened to. sandra February 10, 2009 if you put holes in the lids, then the stuff will leak out. how is this gonna make anyone happy… 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 Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (Posted: yesterday)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: 2 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: 3 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)
Rezurock Lawsuit Claims GVHD Medication Caused Debilitating Skin Condition, Prurigo Nodularis June 12, 2026
Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (Posted: yesterday)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: 2 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: 3 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)