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Cell Phones May Interfere With ICD, Pacemakers, Study Warns June 29, 2015 Martha Garcia Add Your Comments New research examines the risks that individuals with with implanted cardiac devices may face from cellphone interference. Researchers tested recommendations offered by the U.S. Food and Drug Administration (FDA) and other medical institutions concerning the proximity of cellphones with pacemakers and implantable cardioverter defibrillators (ICD). The findings were presented to a joint congress of the European Heart Rhythm Association EHRA, European Society of Cardiology (ESC) and Cardiostim in Milan on June 22, indicating that cellphones may interfere with the cardiac devices, however not as often as previously believed. The researchers indicate that recommendations regarding their use should still be followed. 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 Cell phones emit electromagnetic waves that can potentially affect the performance of pacemakers and ICDs, creating a serious health risk to users. Researchers studied more than 3,400 electromagnetic interference tests on 308 people. Of those 147 had heart implants, 96 with ICDs,and 65 with cardiac resynchronization therapy (CRT) devices. These were tested using three types of smartphones, the Nokia Lumia, Samsung Galaxy 3 and the HTC One XL. Researchers found one out of the 308 participants were affected by electromagnetic interference from smartphones. FDA recommendations for heart implants are to keep a safe distance of 15 to 20 cm between pacemakers or ICDs and cellphones or to use the cell phone on the ear opposite of the side where the implant is located. Study authors say the current recommendations set by the FDA to keep a safe distance should be upheld. Pacemakers can often detect electromagnetic interference from smartphones and interpret that as a cardiac signal, causing the pacemaker to stop working, even if only for a brief moment, putting the patient in danger. Patients experience a disrupted heart rhythm and may suffer syncope. Cellphones can also mimic the signal of the ICD and is often similar to a ventricular tachyarrhythmia causing the ICD to deliver a shock to the patients, causing pain and other life threatening complications. The negative influence of electromagnetic waves on health has been found in other studies, yet researchers wanted data to determine if the recommendations were still relevant. Researchers said while interference between smartphones and cardiac devices is uncommon, it still can occur and is quite dangerous when it does occur. Another recent study published in the medical journal JAMA Internal Medicine highlighted potential concerns associated with the implanted devices, suggesting that many deaths caused by pacemakers and ICDs may be going unnoticed. Written by: Martha Garcia Health & Medical Research Writer Martha Garcia is a health and medical research writer at AboutLawsuits.com with over 15 years of experience covering peer-reviewed studies and emerging public health risks. She previously led content strategy at The Blogsmith and contributes original reporting on drug safety, medical research, and health trends impacting consumers. Tags: ICD, Pacemaker, Smartphone More Lawsuit Stories Dupixent Cancer Lawsuit Filed Over Cutaneous T-Cell Lymphoma (CTCL) Diagnosis December 19, 2025 Lawsuit Alleges Roblox Predator Groomed 13-Year-Old Girl for Explicit Photo Exchange Through Gaming Platform December 19, 2025 Financial Fraud Losses Among Older Adults Increased to $2.4B Last Year: FTC December 19, 2025 0 Comments 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 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 Term Δ MORE TOP STORIES Dupixent Cancer Lawsuit Filed Over Cutaneous T-Cell Lymphoma (CTCL) Diagnosis (Posted: 2 days ago) An Illinois woman diagnosed with stage IV cutaneous T-cell lymphoma (CTCL) after two years of Dupixent injections has filed a lawsuit against the drug manufacturers. 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Dupixent Cancer Lawsuit Filed Over Cutaneous T-Cell Lymphoma (CTCL) Diagnosis (Posted: 2 days ago) An Illinois woman diagnosed with stage IV cutaneous T-cell lymphoma (CTCL) after two years of Dupixent injections has filed a lawsuit against the drug manufacturers. MORE ABOUT: DUPIXENT LAWSUITLawyers Propose Dupixent Lawsuit Be Set for Trial After Dec. 6, 2027 (12/11/2025)Dupixent CTCL Lawsuit Filed Over Diagnosis of Both Mycosis Fungoides and Sezary Syndrome (12/05/2025)Drug Makers Must Respond to Dupixent Lawsuit Over Lymphoma Diagnosis by Jan. 7, 2026 (12/02/2025)
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Depo-Provera Meningioma Warning Update Approved by FDA, As Lawsuits Move Forward (Posted: 4 days ago) The FDA has approved an update to the Depo-Provera drug label to include a warning of the risks of meningioma. MORE ABOUT: DEPO-PROVERA LAWSUITLawsuit Alleges Depo-Provera Neurological Symptoms Were Result of Meningioma (12/12/2025)Court To Weigh Evidence That Depo-Provera Causes Meningioma Tumors in Mid-2026 (12/08/2025)Depo-Provera Lawsuit MDL Status Hearings Scheduled Throughout 2026 (12/01/2025)