Lawsuit Alleges Amazon Nitrous Oxide Canisters Left Customers With Paralysis, Brain Damage, Other Injuries
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.
GreatCall Lively Mobile Recall Issued Due to Risk Emergency Button May Fail September 3, 2019 Russell Maas Add Your CommentsNearly 45,000 Lively Mobile emergency call devices sold by GreatCall have been recalled, due to a risk they may fail to send out an alert even after the button is pushed.The U.S. Consumer Product Safety Commission (CPSC) announced the GreatCall Lively Mobile recall on August 30, after routine testing by the manufacturing company detected the push button may fail to send a signal during an emergency.While no injuries have been linked to the Lively Mobile button failures, many elderly and disabled individuals rely on the device to call for help in the event of a sudden emergency.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 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 COMPENSATIONThe recall impacts Lively Mobile Plus model GCR4 emergency alert devices, which are designed with a call button that is supposed to send a signal for help when pushed. The products are often used by those prone to fall hazards or medical conditions which may require emergency medical response.The devices are worn on a magnetic lanyard around a consumer’s neck to detect falls, or can be clipped on to the individuals pocket or other accessories for convenience to communicate a signal in an emergency or assistance required situation.In the event the device fails to send a call signal, an individual who has experienced a fall or other potentially life-threatening emergency could be stranded without assistance.The recall affects Lively Mobile Plus emergency alert devices with model number GCR4 and date code 19.01 or 19.03. The products were manufactured in China by Borqs Hong Kong Limited and Shenzhen Saidaxin Technology Co. Ltd. They were imported and distributed for sale across the U.S. by GreatCall Inc., of San Diego, California.The devices were sold at Best Buy and Walmart stores nationwide and online at www.greatcall.com and www.amazon.com from April 2019 through May 2019 for between $25 and $50.Customers are being asked to immediately stop using the recalled Lively Mobile Plus devices and contact GreatCall customer service at 800-359-1791 or email them at customerservice@greatcall.com for information on how to receive a full refund. 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 nation’s leading personal injury law firms and oversees the site’s editorial strategy, including SEO and content development. Tags: Medical Alert Device RecallMore Lawsuit Stories Ozempic Vision Loss Lawsuit Highlights Devastating Consequences of NAION Diagnosis May 4, 2026 Lawsuit Alleges Amazon Nitrous Oxide Canisters Left Customers With Paralysis, Brain Damage, Other Injuries May 4, 2026 Social Media Mental Health Lawsuit Alleges Facebook, Other Platforms Contributed to Teen’s Suicide May 4, 2026 0 Comments NameThis 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 Ozempic Vision Loss Lawsuit Highlights Devastating Consequences of NAION Diagnosis (Posted: today)A Massachusetts man has filed an Ozempic vision loss lawsuit claiming the diabetes drug injections caused a condition that eroded his vision in both eyes.MORE ABOUT: OZEMPIC LAWSUITGLP-1 Dementia, Alzheimer’s Disease Risks Questioned in New Study (04/27/2026)GLP-1 Wrongful Death Lawsuit Claims Compounder Sold Contaminated Meds (04/15/2026)Gastrointestinal Problems Are Most Common GLP-1 Side Effects, Study Finds (04/06/2026) NFL Sports Gambling Lawsuit Claims Live Game Data Fueled FanDuel, DraftKings Addiction (Posted: 3 days ago)A public health advocacy group and two Pennsylvania men have filed a lawsuit against FanDuel, DraftKings and the NFL over the use of data for addictive, live in-game microbets.MORE ABOUT: SPORTS BETTING ADDICTION LAWSUITU.S. Lawmakers Introduce Bill To Combat Sports Betting Addiction (05/04/2026)Appeal Challenges Dismissal of DraftKings Lawsuit Over Gambling Addiction (04/27/2026)BetMGM Lawsuit Alleges Gambling Addict’s ‘Self-Exclusion’ Listing Was Not Honored (04/13/2026) Recalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (Posted: 4 days ago)Insulet is removing certain Omnipod 5 insulin pump pods from use following a surge in reports of insulin delivery failures that raise risks of diabetic ketoacidosis and other serious complications.MORE ABOUT: OMNIPOD RECALL LAWSUITInsulet OmniPod 5 Recall Lawsuits May Be Filed Over Problems Resulting in Diabetic Ketoacidosis, Hospitalization and Death (03/24/2026)Omnipod 5 Insulin Pump Recall Follows Reports of Serious Injuries: FDA (03/20/2026)
Lawsuit Alleges Amazon Nitrous Oxide Canisters Left Customers With Paralysis, Brain Damage, Other Injuries May 4, 2026
Social Media Mental Health Lawsuit Alleges Facebook, Other Platforms Contributed to Teen’s Suicide May 4, 2026
Ozempic Vision Loss Lawsuit Highlights Devastating Consequences of NAION Diagnosis (Posted: today)A Massachusetts man has filed an Ozempic vision loss lawsuit claiming the diabetes drug injections caused a condition that eroded his vision in both eyes.MORE ABOUT: OZEMPIC LAWSUITGLP-1 Dementia, Alzheimer’s Disease Risks Questioned in New Study (04/27/2026)GLP-1 Wrongful Death Lawsuit Claims Compounder Sold Contaminated Meds (04/15/2026)Gastrointestinal Problems Are Most Common GLP-1 Side Effects, Study Finds (04/06/2026)
NFL Sports Gambling Lawsuit Claims Live Game Data Fueled FanDuel, DraftKings Addiction (Posted: 3 days ago)A public health advocacy group and two Pennsylvania men have filed a lawsuit against FanDuel, DraftKings and the NFL over the use of data for addictive, live in-game microbets.MORE ABOUT: SPORTS BETTING ADDICTION LAWSUITU.S. Lawmakers Introduce Bill To Combat Sports Betting Addiction (05/04/2026)Appeal Challenges Dismissal of DraftKings Lawsuit Over Gambling Addiction (04/27/2026)BetMGM Lawsuit Alleges Gambling Addict’s ‘Self-Exclusion’ Listing Was Not Honored (04/13/2026)
Recalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (Posted: 4 days ago)Insulet is removing certain Omnipod 5 insulin pump pods from use following a surge in reports of insulin delivery failures that raise risks of diabetic ketoacidosis and other serious complications.MORE ABOUT: OMNIPOD RECALL LAWSUITInsulet OmniPod 5 Recall Lawsuits May Be Filed Over Problems Resulting in Diabetic Ketoacidosis, Hospitalization and Death (03/24/2026)Omnipod 5 Insulin Pump Recall Follows Reports of Serious Injuries: FDA (03/20/2026)