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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 25 of 25 Results
Related Medical Device Recalls
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FDA Recall
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Z-1461-2021 - BIOTRONIK ILIVIA 7, DR-T DF-1 PROMRI, REF 404622, UDI: 04035479142094 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life... 2 04/21/2021 FEI # 1028232
BIOTRONIK Inc
Z-1462-2021 - BIOTRONIK ILIVIA NEO 7 VR-T DF-1 ProMRI, REF 429531, UDI: 04035479156763 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of l... 2 04/21/2021 FEI # 1028232
BIOTRONIK Inc
Z-1463-2021 - BIOTRONIK INTICA NEO 7 VR-T DX DF-1 ProMRI, REF 429559, UDI: 04035479156855 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment o... 2 04/21/2021 FEI # 1028232
BIOTRONIK Inc
Z-1464-2021 - BIOTRONIK ILIVIA NEO 7 DR-T DF-1 ProMRI, REF 429529, UDI: 04035479156749 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of l... 2 04/21/2021 FEI # 1028232
BIOTRONIK Inc
Z-1442-2021 - BIOTRONIK Ilestro 7 DR-T, DF-4, REF383564, UDI: 04035479125202 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threat... 2 04/21/2021 FEI # 1028232
BIOTRONIK Inc
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