BIOTRONIK Inc - BIOTRONIK IPERIA - Class 2 Recall
BIOTRONIK IPERIA 7,VR-T, DX, DF-1, ProMRI, REF 393032, UDI: 04035479129477 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias. (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 22, 2021 Category: Medical Devices Source Type: alerts
BIOTRONIK Inc - BIOTRONIK Iforia - Class 2 Recall
BIOTRONIK Iforia 7,DR-T, DF-1,REF 390064, UDI: 04035479126926 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias. (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 22, 2021 Category: Medical Devices Source Type: alerts
BIOTRONIK Inc - BIOTRONIK ILESTO 7 VRT - Class 2 Recall
BIOTRONIK Ilestro 7 VR-T, DF-1, REF 383578, UDI: 04035479125349 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias. (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 22, 2021 Category: Medical Devices Source Type: alerts
BIOTRONIK Inc - BIOTRONIK ITREVIA - Class 2 Recall
BIOTRONIK ITREVIA 7, VR-T DF-1, REF 393040, UDI: 04035479129552 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias. (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 22, 2021 Category: Medical Devices Source Type: alerts
BIOTRONIK Inc - BIOTRONIK ILESTO 7 DRT - Class 2 Recall
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-threatening ventricular arrhythmias. (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 22, 2021 Category: Medical Devices Source Type: alerts
BIOTRONIK Inc - BIOTRONIK ILIVIA - Class 2 Recall
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-threatening ventricular arrhythmias. (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 22, 2021 Category: Medical Devices Source Type: alerts
BIOTRONIK Inc - BIOTRONIK INTICA - Class 2 Recall
BIOTRONIK INTICA NEO 7 HF-T DF-1 IS-1 ProMRI, REF 429553, UDI: 04035479156831 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias. (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 22, 2021 Category: Medical Devices Source Type: alerts
BIOTRONIK Inc - BIOTRONIK INTICA - Class 2 Recall
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 of life-threatening ventricular arrhythmias. (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 22, 2021 Category: Medical Devices Source Type: alerts
BIOTRONIK Inc - BIOTRONIK ILIVIA - Class 2 Recall
BIOTRONIK ILIVIA 7, VR-T DF-1 ProMRI, REF 404625, UDI: 04035479142124 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias. (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 22, 2021 Category: Medical Devices Source Type: alerts
BIOTRONIK Inc - BIOTRONIK Iperia - Class 2 Recall
BIOTRONIK Iperia 7, DR-T, DF-1, ProMRI REF 392409, UDI: 04035479128777 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias. (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 22, 2021 Category: Medical Devices Source Type: alerts
BIOTRONIK Inc - BIOTRONIK ITREVIA - Class 2 Recall
BIOTRONIK ITREVIA 7, VR-T DF-4, REF 393041, UDI: 04035479129569 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias. (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 22, 2021 Category: Medical Devices Source Type: alerts
BIOTRONIK Inc - BIOTRONIK ILESTO 7 VRT - Class 2 Recall
BIOTRONIK Ilestro 7 VR-T DX, DF-1, REF 383594, UDI: 04035479125509 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias. (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 22, 2021 Category: Medical Devices Source Type: alerts
BIOTRONIK Inc - BIOTRONIK ILESTO 7 VRT - Class 2 Recall
BIOTRONIK Ilestro 7 VR-T, DF-4, REF 383580, UDI: 04035479125363 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias. (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 22, 2021 Category: Medical Devices Source Type: alerts
BIOTRONIK Inc - BIOTRONIK ILIVIA - Class 2 Recall
BIOTRONIK ILIVIA 7, VR-T DF4 ProMRI, REF 404626, UDI: 04035479142131 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias. (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 22, 2021 Category: Medical Devices Source Type: alerts
BIOTRONIK Inc - BIOTRNIK ITREVIA - Class 2 Recall
BIOTRONIK ITREVIA 7, DR-T QP DF-1, REF 392412, UDI: 04035479128807 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias. (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 22, 2021 Category: Medical Devices Source Type: alerts
