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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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Class
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FDA Recall
Posting Date
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Recalling Firm
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Z-0916-2009 - Cardiac Science Powerheart Automated External Defibrillator G3 9300A 2 02/25/2009 Cardiac Science Corporation
Z-0917-2009 - Cardiac Science First Save Automated External Defibrillator G3 9300C 2 02/25/2009 Cardiac Science Corporation
Z-0918-2009 - Cardiac Science Powerheart Automated External Defibrillator G3 9300E. 2 02/25/2009 Cardiac Science Corporation
Z-0922-2009 - GE Responder 2019198 AED Manufactured for GE Medical Systems Information Technologies by Cardiac Science Corporation, Automated External Defibrillator 2 02/25/2009 Cardiac Science Corporation
Z-0920-2009 - Cardiac Science Powerheart Automated External Defibrillator G3 9390E 2 02/25/2009 Cardiac Science Corporation
Z-0921-2009 - Cardio Vive 92532 AED, BURDICK Manufactured by Cardiac Science Corporation, Automated External Defibrillator 2 02/25/2009 Cardiac Science Corporation
Z-0919-2009 - Cardiac Science Powerheart Automated External Defibrillator G3 9390A 2 02/25/2009 Cardiac Science Corporation
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