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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 14 Results
Related Medical Device Recalls
 
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Product Description
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FDA Recall
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Z-0765-2010 - Cardiac Science 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 approp... 1 03/04/2010 Cardiac Science Corporation
Z-0766-2010 - Cardiac Science Powerheart 9300C 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 a... 1 03/04/2010 Cardiac Science Corporation
Z-0767-2010 - Cardiac Science Powerheart 9300D 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 a... 1 03/04/2010 Cardiac Science Corporation
Z-0768-2010 - Cardiac Science 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 a... 1 03/04/2010 Cardiac Science Corporation
Z-0769-2010 - Cardiac Science 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... 1 03/04/2010 Cardiac Science Corporation
Z-0770-2010 - Cardiac Science 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 approp... 1 03/04/2010 Cardiac Science Corporation
Z-0778-2010 - NK 9200G. CardioLife 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).... 1 03/04/2010 Cardiac Science Corporation
Z-0772-2010 - Burdick Cardiovive 92531 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 appropria... 1 03/04/2010 Cardiac Science Corporation
Z-0773-2010 - Burdick 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 appropria... 1 03/04/2010 Cardiac Science Corporation
Z-0774-2010 - Burdick Cardiovive 92533 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 appropria... 1 03/04/2010 Cardiac Science Corporation
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