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.
Playtex Breast Pump Recall Issued for Power Adapters Due to Shock Risk March 20, 2014 Russell Maas Add Your CommentsPlaytex has issued a recall for power adapters used with certain breast pump products, after determining that the adapters may loosen from the pump and pose a risk of electric shocks for users.The Playtex breast pump recall was announced by the FDA on March 18, impacting certain Nurser Delux Double Electric Breast Pumps with AC/DC power adapters.The manufacturer indicates that the casing on the adapters may become loose and possibly separate from the pump. Although no reports have been received of injuries or incidents, these problems could pose an electrical shock hazard.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 recall includes Playtex Nurser Deluxe Double Electric Breast Pumps with serial numbers ranging between P12324-XXXX and P13205-XXXX and production code numbers ranging between 1241 and 1324. The adapters were sold exclusively with the purchase of the Playtex Nurser Deluxe Double Breast Pump.The affected nursing pumps were manufactured by Energizer Personal Care, Playtex Manufacturing, Inc. of Sheldon Connecticut where they were sold nationwide at specialty stores and online retailers.The agency encourages customers to be cautious of the products and if the user notices any signs that the adapter is coming loose they should stop using the product immediately and contact Playtex at 1-888-207-1429 or visit them online at www.playtexproducts.com.Adverse events linked to the breast pumps can be submitted to the FDA’s MedWatch Adverse Event Reporting program. 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: Breast Pump, Electrocution, Playtex Image Credit: |More Lawsuit Stories AngioDynamics Port Catheter Lawsuit Claims Womanโs SmartPort Implants Caused Multiple Infections June 23, 2026 Litigation Over LINX Surgery Problems Underway in Lawsuit Against Acid Reflux Device Manufacturer June 23, 2026 Pfizer Settles Oxbryta Lawsuit Over Childโs Vaso-Occlusive Crises (VOCs) Linked To Recalled Drug June 23, 2026 0 Comments EmailThis 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 AngioDynamics Port Catheter Lawsuit Claims Womanโs SmartPort Implants Caused Multiple Infections (Posted: today)A Georgia woman has filed an AngioDynamics port catheter lawsuit alleging two SmartPort implants caused repeated infections requiring multiple surgeries.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITXcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis (06/12/2026)Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (06/03/2026)SmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body (05/15/2026) Paraquat MDL Judge Requires Settlement Holdouts To Meet With Special Master (Posted: yesterday)Plaintiffs who have yet to decide to participate in a Paraquat lawsuit settlement agreement must meet with a Special Master overseeing negotiations within the next 30 days.MORE ABOUT: PARAQUAT PARKINSON’S DISEASE LAWSUITSInformation on Paraquat Settlement Offers To Be Provided to Special Master, MDL Judge Orders (04/09/2026)As Paraquat Parkinsonโs Disease Cases Continue To Emerge, Syngenta Will Halt Herbicide’s Production (03/09/2026)Risk of Parkinsonโs Disease From Paraquat Lead to Calls To Ban Weed Killer (02/11/2026) Suboxone Dry Mouth Lawsuit Claims Dental Problems Could Have Been Avoided With Sublocade Shot (Posted: 5 days ago)Five plaintiffs say they all suffered dental problems due to the side effects of Suboxone, which could have been avoided with adequate warnings.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (06/11/2026)Suboxone 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)
AngioDynamics Port Catheter Lawsuit Claims Womanโs SmartPort Implants Caused Multiple Infections June 23, 2026
Litigation Over LINX Surgery Problems Underway in Lawsuit Against Acid Reflux Device Manufacturer June 23, 2026
Pfizer Settles Oxbryta Lawsuit Over Childโs Vaso-Occlusive Crises (VOCs) Linked To Recalled Drug June 23, 2026
AngioDynamics Port Catheter Lawsuit Claims Womanโs SmartPort Implants Caused Multiple Infections (Posted: today)A Georgia woman has filed an AngioDynamics port catheter lawsuit alleging two SmartPort implants caused repeated infections requiring multiple surgeries.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITXcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis (06/12/2026)Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (06/03/2026)SmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body (05/15/2026)
Paraquat MDL Judge Requires Settlement Holdouts To Meet With Special Master (Posted: yesterday)Plaintiffs who have yet to decide to participate in a Paraquat lawsuit settlement agreement must meet with a Special Master overseeing negotiations within the next 30 days.MORE ABOUT: PARAQUAT PARKINSON’S DISEASE LAWSUITSInformation on Paraquat Settlement Offers To Be Provided to Special Master, MDL Judge Orders (04/09/2026)As Paraquat Parkinsonโs Disease Cases Continue To Emerge, Syngenta Will Halt Herbicide’s Production (03/09/2026)Risk of Parkinsonโs Disease From Paraquat Lead to Calls To Ban Weed Killer (02/11/2026)
Suboxone Dry Mouth Lawsuit Claims Dental Problems Could Have Been Avoided With Sublocade Shot (Posted: 5 days ago)Five plaintiffs say they all suffered dental problems due to the side effects of Suboxone, which could have been avoided with adequate warnings.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (06/11/2026)Suboxone 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)