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 ...
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 ...
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 ...
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 ...
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 ...
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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 ...
Defibrillator clocks keep inaccurate time, complicating efforts to determine mortality risk and resu
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 ...
SAN FRANCISCO (MarketWatch) -- Medtronic Inc. said late Thursday that it is voluntarily advising physicians about a potential battery shorting mechanism that may occur in a subset of implantable ...
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