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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 25 Results
510(K) Number: K040438
 
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FDA Recall
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Responder 2023440 automated external defibrillator. This semi-automatic model requires the user t... 2 04/06/2010 Cardiac Science Corporation
Powerheart Automated External Defibrillator (AED), G3 is indicated for emergency treatment of victim... 2 09/19/2011 Cardiac Science Corporation
Powerheart AED G3 Automated External Defibrillator Model 9300A (Automatic). Cardiac Science AEDs ar... 2 03/02/2006 Cardiac Science Corporation
Powerheart AED G3 Automated External Defibrillator Model 9300A (Automatic). Cardiac Science AEDs ar... 2 01/15/2005 Cardiac Science, Inc.
Powerheart 9390E automated external defibrillator. This semi-automatic model requires the user to... 2 04/06/2010 Cardiac Science Corporation
Powerheart 9390A automated external defibrillator. This fully automatic model does not require th... 2 04/06/2010 Cardiac Science Corporation
Powerheart 9300P automated external defibrillator. This semi-automatic model requires the user to... 2 04/06/2010 Cardiac Science Corporation
Powerheart 9300E automated external defibrillator. This semi-automatic model requires the user to... 2 04/06/2010 Cardiac Science Corporation
Powerheart 9300A automated external defibrillator. This fully automatic model does not require the ... 2 04/06/2010 Cardiac Science Corporation
NK 9231 CardioLife automated external defibrillator. This semi-automatic model requires the user to... 1 03/04/2010 Cardiac Science Corporation
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