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Saturday, February 06, 2010 CAUTION URGED ON POWERHEART AND CARDIOVIVE AUTOMATED EXTERNAL DEFIBRILLATORS |
The Food and Drug Administration (FDA) is alerting users of certain Powerheart and CardioVive automated external defibrillators that these devices may malfunction unexpectedly. This can cause a failure to deliver the electric shocks that are needed to treat sudden cardiac arrest or arrhythmias. |
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