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.
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.
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.
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.
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
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.
Change Healthcare Lawsuit Lawyers are reviewing Change Healthcare class action lawsuits for individuals who had their personal information stolen due to the data breach.
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.
AngioDynamics Port Catheter 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.
Processed Food Lawsuit Lawsuits are being pursued against the food industry over their manufacturing and advertising of ultra-processed foods, which have caused a generation of children to face an increased risk of developing childhood diabetes and other chronic illnesses.
FDA Issues “Do Not Use” Warning for Certain UV Wands Due to Radiation Risks Safe-T-Lite, OttLite, Uvilizer, SurfaceSoap and other types of UV disinfecting wands may expose users to unhealthy levels of radiation. August 23, 2023 Katherine McDaniel Add Your Comments Federal regulators have issued an updated warning advising consumers not to use 13 different ultraviolet (UV) wands, which are marketed as products that can quickly disinfect or sanitize objects, since they may expose users to potentially dangerous levels of radiation. The U.S. Food and Drug Administration (FDA) issued the UV wand safety warning on August 17, and provided a current list of UV wand products that pose serious radiation risks. UV wands are marketed to consumers as handheld devices that disinfect surfaces using UV-C radiation. They are designed to be held a few inches from an object to sanitize them within seconds. The agency initially issued a UV wand warning in July 2022, after sample testing confirmed that several UV wand products advertised as safe for consumer use were emitting high levels of radiation. UV Wand Radiation Risks FDA officials warn that they have confirmed, through testing of samples collected from multiple manufacturers, that at least 13 UV wands sold in the U.S. may emit unsafe levels of UV-C radiation, and can expose consumers to radiation levels 3,000 times higher than the recommended exposure limit. According to the FDA, humans are only exposed to UV-C radiation by artificial means, such as a laser or lamp, as the radiation is blocked by the earth’s ozone layer. UV-C radiation is the highest energy portion on the spectrum, and exposure to it can result in severe eye injuries or burns to the skin, even after very short durations. The agency warns UV wands can emit UV-C radiation to a distance of up to two inches and expose the device’s user and any nearby individual to dangerous levels of radiation. According to the warning, the wands can expose consumers to unsafe levels of radiation after only a few seconds of use, and can cause serious eye or skin injuries. The FDA warning includes an updated list of UV wand products confirmed by the agency to release unhealthy amounts of radiation, determining they are unsafe for consumers to use: Safe•T•Lite, manufactured by Max-lux Corporation OttLite Rechargeable UVC Disinfecting Wand, model: UV10002M, manufactured by OttLite Technologies Inc. OttLite Compact Travel Disinfecting Wand, model: UV11001M, manufactured by OttLite Technologies Inc. UVILIZER Flip, model: SG-153, manufactured by In My Bathroom LLC, dba IMB Purple Glow Ultraviolet Sterilamp, model: BP52, manufactured by In My Bathroom LLC, dba IMB UVILIZER UV Light Sanitizer, model: Razor, manufactured by In My Bathroom LLC, dba IMB Ultraviolet Sterilamp, model: PURPLEGLOW, manufactured by Vanelc Sharper Image® UV Sanitizing Portable Wand, model: 101362, manufactured by MerchSource LLC SurfaceSoap UV, manufactured by PhoneSoap LLC Magic UV Light SanitizerTM, manufactured by Magic UV Light Sanitizer WBM Smart UV Portable Sterilizer, model: UV-03, manufactured by World Business Management (WBM) Safe and Healthy Disinfecting UV Light, model: 2090, manufactured by Ontel Products Corporation 59S® Wand Disinfector, model: 5F1025917, manufactured by Shenzhen UV Guard Technology Co., Ltd. The FDA has expressed skepticism over the manufacturers’ claims that the wands can safely disinfect objects in a matter of seconds. It has also expressed concern over the lack of safety precautions that should have been in place to protect consumers from unnecessary radiation exposure, such as safety information, product use instructions, and features that reduce the emission of radiation. The agency has issued Notice of Defect letters to several UV wand manufacturers, notifying them of the safety risks involved with use of their products, and warning them to take corrective action to address the issue. The letters required the manufacturers to submit a written response to the FDA immediately with the number of products they sold, and where the units were distributed. The agency also requested manufacturers to create plans to take corrective actions, notify consumers of the product defects, and provide consumers with a replacement or refund. The FDA is currently working with each manufacturer to ensure they are implementing adequate measures to take corrective actions toward resolving the safety issues. Do You Know about… SPORTS BETTING ADDICTION LAWSUITS FOR YOUNG ADULTS Gambling addiction and severe financial losses have been linked to popular sports betting platforms like DraftKings, FanDuel, and Caesars. Lawsuits are being filed by young adults and students who were targeted by deceptive promotions, addictive app features, and aggressive marketing tactics. See if you qualify for a sports betting addiction lawsuit. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Do You Know About… SPORTS BETTING ADDICTION LAWSUITS FOR YOUNG ADULTS Gambling addiction and severe financial losses have been linked to popular sports betting platforms like DraftKings, FanDuel, and Caesars. Lawsuits are being filed by young adults and students who were targeted by deceptive promotions, addictive app features, and aggressive marketing tactics. See if you qualify for a sports betting addiction lawsuit. Learn More SEE IF YOU QUALIFY FOR COMPENSATION UV Wand Safety Recommendations Consumers are urged to stop using the handheld UV wand products, and use an alternative method to sanitize surfaces, such as using a chemical disinfecting solution. The FDA recommends consumers use protective measures if they decide to use a UV-C radiation-emitting product and follow the product’s safety instructions to protect their eyes and skin from exposure. The FDA also recommends consumers avoid any UV-C emitting product that does not include safety information on the radiation emitted or product use instructions. For additional information, consumers may email their questions to the Division of Industry and Consumer Education (DICE) at DICE@FDA.HHS.GOV, or call 800-638-2041 or 301-796-7100. The FDA also calling for consumers, health care professionals, and manufacturers to report any incidents or hazardous events involving a UV wand or UV emitting product using the MedWatch Voluntary Reporting Form, Accidental Radiation Occurrence Report Form, or Allegations of Regulatory Misconduct Form. Tags: Disinfectant, Eye Injury, Radiation, Radiation Exposure, Skin Irritation, Skin Reactions, UV Wands More Lawsuit Stories Depo-Provera Lawsuit Sign Ups Expected To Continue as First Brain Tumor Cases Prepared for Trial May 23, 2025 Uber Seeks To Transfer MDL Sexual Assault Lawsuits to Districts Where Attacks Occurred for Trial May 23, 2025 Oxbryta Recall Lawsuit Alleges Sickle Cell Drug Increased Frequency of Dangerous VOCs May 23, 2025 0 Comments 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 No Post Comment I authorize the above comments be posted on this page Weekly 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 TermCommentsThis field is for validation purposes and should be left unchanged. Δ MORE TOP STORIES Depo-Provera Lawsuit Sign Ups Expected To Continue as First Brain Tumor Cases Prepared for Trial (Posted: today) After a growing body of evidence has linked use of the Depo-Provera birth control shot to an increased risk of brain tumors, thousands of women nationwide are seeking information on how to sign up for the Depo-Provera lawsuit. MORE ABOUT: DEPO-PROVERA LAWSUITCourt Outlines Requirements for Depo-Provera Lawsuit Proof of Use, Type of Meningioma Tumor (05/15/2025)Depo Shot Lawsuit Filed Over Serious Brain Tumor Injuries (05/07/2025)Lawsuit Alleges Depo-Provera Migraines, Headaches Led to Meningioma Brain Tumor Diagnosis (05/01/2025) Lawyers To Select 50 Suboxone Dental Lawsuits for Next Phase of MDL Bellwether Discovery (Posted: yesterday) As lawyers continue to review records on more than 500 Suboxone tooth decay lawsuits, the MDL judge has outlined the process for identifying a smaller group that will move into the next discovery phase. MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUIT500 Suboxone Tooth Decay Cases Randomly Selected for Bellwether Record Collection Pool (04/24/2025)Status of Suboxone Tooth Loss Lawsuits To Be Reviewed at MDL Conference (04/16/2025)Prenatal Opioid Exposure May Result in Smaller Brains Among Newborns: Study (04/14/2025) Hair Relaxer Lawsuits MDL Judge Seeks Status Report on Discovery Proceedings (Posted: 2 days ago) A federal judge wants lawyers involved in hair relaxer lawsuits to provide an update this week on the status of discovery proceedings for a pool of cases being considered for bellwether trial dates. MORE ABOUT: HAIR RELAXER LAWSUITFormaldehyde Found in Range of Personal Care Products Used Primarily by Black and Latina Women (05/14/2025)Lawyers Selected 32 Hair Relaxer Lawsuits for Bellwether Discovery in MDL (05/13/2025)Hair Relaxer Settlement Master Appointed To Oversee Negotiations To Resolve Cancer Lawsuits (04/29/2025)
Depo-Provera Lawsuit Sign Ups Expected To Continue as First Brain Tumor Cases Prepared for Trial May 23, 2025
Uber Seeks To Transfer MDL Sexual Assault Lawsuits to Districts Where Attacks Occurred for Trial May 23, 2025
Depo-Provera Lawsuit Sign Ups Expected To Continue as First Brain Tumor Cases Prepared for Trial (Posted: today) After a growing body of evidence has linked use of the Depo-Provera birth control shot to an increased risk of brain tumors, thousands of women nationwide are seeking information on how to sign up for the Depo-Provera lawsuit. MORE ABOUT: DEPO-PROVERA LAWSUITCourt Outlines Requirements for Depo-Provera Lawsuit Proof of Use, Type of Meningioma Tumor (05/15/2025)Depo Shot Lawsuit Filed Over Serious Brain Tumor Injuries (05/07/2025)Lawsuit Alleges Depo-Provera Migraines, Headaches Led to Meningioma Brain Tumor Diagnosis (05/01/2025)
Lawyers To Select 50 Suboxone Dental Lawsuits for Next Phase of MDL Bellwether Discovery (Posted: yesterday) As lawyers continue to review records on more than 500 Suboxone tooth decay lawsuits, the MDL judge has outlined the process for identifying a smaller group that will move into the next discovery phase. MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUIT500 Suboxone Tooth Decay Cases Randomly Selected for Bellwether Record Collection Pool (04/24/2025)Status of Suboxone Tooth Loss Lawsuits To Be Reviewed at MDL Conference (04/16/2025)Prenatal Opioid Exposure May Result in Smaller Brains Among Newborns: Study (04/14/2025)
Hair Relaxer Lawsuits MDL Judge Seeks Status Report on Discovery Proceedings (Posted: 2 days ago) A federal judge wants lawyers involved in hair relaxer lawsuits to provide an update this week on the status of discovery proceedings for a pool of cases being considered for bellwether trial dates. MORE ABOUT: HAIR RELAXER LAWSUITFormaldehyde Found in Range of Personal Care Products Used Primarily by Black and Latina Women (05/14/2025)Lawyers Selected 32 Hair Relaxer Lawsuits for Bellwether Discovery in MDL (05/13/2025)Hair Relaxer Settlement Master Appointed To Oversee Negotiations To Resolve Cancer Lawsuits (04/29/2025)