A faulty component in about 280,000 external defibrillators may not work properly when the devices are used to reverse cardiac arrest, according to a warning from the Food and Drug Administration.
The warning covers 14 different kinds of devices made by GE Responder, CardioVive, Powerheart and Nihon Kohden. They all contain a faulty part made by Cardiac Science Corp. of Washington state. The FDA is recommending patients and health care providers use different defibrillators.
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