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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 7 of 7 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Recalling Firm
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Z-1243-2010 - Powerheart 9300A automated external defibrillator. This fully automatic model does not require the user to press a shock button in order for the device to deliver therapy (when appropriate). Brand... 2 04/06/2010 Cardiac Science Corporation
Z-1244-2010 - Powerheart 9300E automated external defibrillator. This semi-automatic model requires the user to press a shock button in order for the device to deliver defibrillation energy (when appropriate). ... 2 04/06/2010 Cardiac Science Corporation
Z-1245-2010 - Powerheart 9300P automated external defibrillator. This semi-automatic model requires the user to press a shock button in order for the device to deliver defibrillation energy (when appropriate). ... 2 04/06/2010 Cardiac Science Corporation
Z-1249-2010 - Cardiovive 92532 automated external defibrillator. This semi-automatic model requires the user to press a shock button in order for the device to deliver defibrillation energy (when appropriate). ... 2 04/06/2010 Cardiac Science Corporation
Z-1247-2010 - Powerheart 9390E automated external defibrillator. This semi-automatic model requires the user to press a shock button in order for the device to deliver defibrillation energy (when appropriate). ... 2 04/06/2010 Cardiac Science Corporation
Z-1248-2010 - Responder 2023440 automated external defibrillator. This semi-automatic model requires the user to press a shock button in order for the device to deliver defibrillation energy (when appropriate). ... 2 04/06/2010 Cardiac Science Corporation
Z-1246-2010 - Powerheart 9390A automated external defibrillator. This fully automatic model does not require the user to press a shock button in order for the device to deliver therapy (when appropriate). Bra... 2 04/06/2010 Cardiac Science Corporation
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