The FDA has urged providers to exercise additional caution in the use of certain models of the CardioVive automated external defibrillators due to defective components. According to an agency document ...

BOSTON – Boston Scientific Corp. on Monday said it is recalling some defibrillator and pacemaker models that could fail because of an electrical flaw. The recall is the latest in a string of product ...

June 27, 2006 — The US Food and Drug Administration (FDA) and Guidant Cardiac Rhythm Management (a Boston Scientific company) have notified healthcare professionals via letter regarding the potential ...

BOSTON – Newly unsealed court documents show Guidant Corp. drafted a letter warning doctors of a dangerous electrical malfunction in some of its devices designed to restore a normal heartbeat, but the ...

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A second safety warning from Guidant Corp., one of the nation’s largest medical device manufacturers, urged doctors to stop using five defibrillator models because they could malfunction and may have ...

New York, July 31, 2020 (GLOBE NEWSWIRE) -- Reportlinker.com announces the release of the report "Implantable Cardioverter Defibrillators (Cardiovascular) - Global Market Analysis and Forecast Model ...

Chicago, IL - Many models of cardiac defibrillators do not keep accurate time and cannot be relied on to determine collapse-to-defibrillation interval, potentially jeopardizing efforts to assess ...

As many as 750,000 heart devices made by Medtronic PLC contain a serious cybersecurity vulnerability that could let an attacker with sophisticated insider knowledge harm a patient by altering ...