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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 23 Results
510(K) Number: K052161
 
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FDA Recall
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Powerheart Automated External Defibrillator (AED), G3 is indicated for emergency treatment of victim... 2 09/19/2011 Cardiac Science Corporation
Responder 2023440 automated external defibrillator. This semi-automatic model requires the user t... 2 04/06/2010 Cardiac Science Corporation
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
Cardiovive 92532 automated external defibrillator. This semi-automatic model requires the user to... 2 04/06/2010 Cardiac Science Corporation
Burdick Cardiovive 92533 automated external defibrillator. This semi-automatic model requires the u... 1 03/04/2010 Cardiac Science Corporation
GE Responder 2019198 automated external defibrillator. This semi-automatic model requires the user ... 1 03/04/2010 Cardiac Science Corporation
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