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.
FDA Warns Recalled Mighty Bliss Heating Pads Carry Risk of Severe Injury and DeathThe recalled Mighty Bliss Heating Pads have been linked to 31 reports of injuries from shocks, burns and skin irritation December 22, 2022 Russell Maas Add Your CommentsFederal safety regulators have reclassified a Mighty Bliss heating pad recall, giving it Class I designation after hundreds of adverse reports have been identified among users of the defective heating pads, including incidents of users suffering electrical shocks and burns that could result in serious injury or death.More than 500,000 heating pads sold on Amazon.com and Walmart.com under the “Mighty Bliss” brand name were originally pulled from the market in October, with health officials warning consumers to stop using the devices immediately and to unplug them, due to the risk that the heating pads may overheat or spark, which could lead to burn injuries and fire hazards.Mighty Bliss heating pads are designed to be flexible, so they can contour around areas of the body while providing heat through electrical elements. The devices are filled with a gel, fluid, or vegetable matter to help distribute the heat evenly across the heating pad surface to provide temporary relief of aches and pains. However, by October 2022, the agency had become aware of at least 286 consumer complaints of users reporting the devices overheating, sparking, burning or experiencing other electrical problems, which had resulted in 31 injuries, such as shocks, burns, rashes or other irritations.While no explanation was initially given as to why the devices may spark or overheat, it appeared the problem was related to defective electrical components that could reach much higher levels of heat than intended, or cause shock hazards. The FDA warned that use of the recalled electric heating pads can lead to electric shock, skin irritation, rashes, blisters, or burns. Severe burns may lead to skin infection or the formation of scar tissue.Although no additional reports of injury have been disclosed, the FDA upgraded the Mighty Bliss heating pad recall to a Class I recall on December 20, 2022.A Class I recall status is the most serious of its kind, and means that the use of a product has a high probability of causing of causing serious injuries or death.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 544,212 Mighty Bliss electric heating pads manufactured between Jan 8, 2021 to Jan 3, 2022, and distributed from July 29, 2021 through July 21, 2022 throughย Amazon.comย andย Walmart.com.Affected model numbers include:MB-001 (NA-H1121B): large (21โ x 24โ) Blue Electric Heating PadMB-002 )NA-H21C): Extra-large (20โ x 24โ) Blue Electric Heating PadPE-MtyBls-HeatPad-12ร24-Gry-V2(NA-H1121B): Large (12โ X 24โ) Grey Electric Heating PadProduct lots range from 210108 to 220103 and can be found on the recall website. Product model and lot numbers can be found on the Mighty Bliss heating pad label listed in black text beneath the product instructions.In the updated heating pad recall notice, officials are recommending that customers take the following actions:Check your heating pad to determine if you have a recalled Mighty Bliss electric heating pad. If you have this product, stop using it and follow the recommendations in theย recall notice.Do NOT use the recalled Mighty Bliss electric heating pads.Do NOT purchase the recalled Mighty Bliss electric heating pads.Verify receipt of the recall notification at the Whele LLC website:ย https://www.mightyblissheatingpadrecall.expertinquiry.comย even if you no longer have the product on hand.Consumers with questions about the recall are being encouraged to contact Whele LLC at ย 866-918-8768. Consumers who have experienced adverse reactions or quality problems linked to the recalled product can report the concerns to the FDAโsย MedWatchย 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: Burns, Heating Pad Recall, Skin IrritationMore Lawsuit Stories SmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body May 15, 2026 Therapeutic Heating Pad Lawsuit Alleges Amazon Device Overheated, Burned User May 15, 2026 FDA Issues Additional Tazverik Blood Cancer Warnings After Market Recall May 15, 2026 0 Comments URLThis 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 SmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body (Posted: 3 days ago)A Missouri woman alleges her AngioDynamics SmartPort catheter fractured and left a broken piece near her heart, requiring surgical removal after it was found during a CT scan.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUIT18 AngioDynamics Port Catheter Lawsuits Will Be Selected for Bellwether Discovery in August 2026 (05/05/2026)AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism (04/30/2026)Vortex Port Lawsuit Filed After Port Catheter Removed Due to Infection, Blood Clots (04/09/2026) Enfamil NEC Lawsuit Cleared For MDL Trial in July 2026 (Posted: 4 days ago)A federal judge has selected an Enfamil lawsuit to serve as the first NEC infant formula bellwether trial, which is set to begin in July.MORE ABOUT: ENFAMIL AND SIMILAC BABY FORMULA LAWSUITLawsuit Claims Cowโs Milk-Based Baby Formula Use Resulted in Infant Suffering Devastating NEC Symptoms (05/08/2026)Mead Johnson Lawsuit Claims Premature Child Developed NEC From Enfamil (04/24/2026)Similac NEC Lawsuit Payout Increased by $17M in Punitive Damages (04/14/2026) Abbott Eterna Lawsuit Alleges Spinal Cord Stimulator Malfunction Resulted in Worsening Pain (Posted: 5 days ago)According to a lawsuit brought against the manufacturer and the FDA, an Abbott Eterna spinal cord stimulator has caused pain, shocks and complications instead of the relief promised.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Stimulator Lawsuit Alleges SCS Lead Failure Caused Nerve Damage (05/06/2026)Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (04/29/2026)JPML Sets Hearing Over Spinal Cord Stimulator Lawsuit Consolidation for May 28 (04/24/2026)
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