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Cell Phones May Interfere With ICD, Pacemakers, Study Warns June 29, 2015 Martha Garcia Add Your CommentsNew research examines the risks that individuals with with implanted cardiac devices may face from cellphone interference.ย 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…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 COMPENSATIONCell 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 GarciaHealth & Medical Research WriterMartha 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, SmartphoneMore Lawsuit Stories Depo-Provera Meningioma Warning Update Should Be Added to Birth Control Shot: Lawsuit April 22, 2026 Lyft Driver Assault Lawsuit Claims Rideshare Service Performs Inadequate Background Checks Despite Similar Attacks April 22, 2026 Lawsuit Alleges Unsafe Conditions at Planet Fitness Gym Resulted in Womanโs Injuries April 22, 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 Depo-Provera Meningioma Warning Update Should Be Added to Birth Control Shot: Lawsuit (Posted: today)A Depo-Provera meningioma lawsuit argues that Pfizer had a duty to warn women about scientific evidence linking the birth control shot to potential brain tumor growth yet failed to do so.MORE ABOUT: DEPO-PROVERA LAWSUITHearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (04/15/2026)High-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (04/06/2026)Depo-Provera Meningioma Lawyers Reappointed to MDL Leadership Roles (03/25/2026) Judges Will Consider MDL for Dupixent Cancer Lawsuits Late Next Month (Posted: yesterday)A group of federal judges will determine whether all Dupixent cancer lawsuits should be formed into a multidistrict litigation, following oral arguments set for May 28.MORE ABOUT: DUPIXENT LAWSUITDupixent Injections Caused Peripheral T-Cell Lymphoma (PTCL) Diagnosis: Lawsuit (04/06/2026)Link Between Dupixent and CTCL Withheld From Users, Medical Community: Lawsuit (03/31/2026)Drug Makers Agree Dupixent Cancer Lawsuits Should Be Centralized in MDL (03/26/2026) SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation (Posted: 2 days ago)A product liability lawsuit alleges unlicensed Abbott representatives made real-time spinal cord stimulator programming decisions based on a Texas womanโs responses, improperly modifying the device and contributing to her injuries.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITWaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (04/14/2026)Boston Scientific Neuromodulation Lawsuit Claims Spinal Cord Stimulator Exacerbated Chronic Pain (04/08/2026)Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (04/03/2026)
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