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Rivacor 3 DR-T DF4 ProMRI

BIOTRONIK SE & Co. KG · Model 429573 · UDI-DI 04035479156992

MRM Prescription
0
510(k) clearances
7,836
Adverse events (191 deaths)
34
Recalls
6
Facilities

Recalls

DateFirmReason
2021-03-08BIOTRONIK IncThere is a potential for premature battery depletion in Implantable Cardioverter Defibrillators and Cardiac Resynchronization Therapy Defibrillators (CRT'Ds)
2021-03-08BIOTRONIK IncThere is a potential for premature battery depletion in Implantable Cardioverter Defibrillators and Cardiac Resynchronization Therapy Defibrillators (CRT'Ds)
2021-03-08BIOTRONIK IncThere is a potential for premature battery depletion in Implantable Cardioverter Defibrillators and Cardiac Resynchronization Therapy Defibrillators (CRT'Ds)
2021-03-08BIOTRONIK IncThere is a potential for premature battery depletion in Implantable Cardioverter Defibrillators and Cardiac Resynchronization Therapy Defibrillators (CRT'Ds)
2021-03-08BIOTRONIK IncThere is a potential for premature battery depletion in Implantable Cardioverter Defibrillators and Cardiac Resynchronization Therapy Defibrillators (CRT'Ds)
2021-03-08BIOTRONIK IncThere is a potential for premature battery depletion in Implantable Cardioverter Defibrillators and Cardiac Resynchronization Therapy Defibrillators (CRT'Ds)
2021-03-08BIOTRONIK IncThere is a potential for premature battery depletion in Implantable Cardioverter Defibrillators and Cardiac Resynchronization Therapy Defibrillators (CRT'Ds)
2021-03-08BIOTRONIK IncThere is a potential for premature battery depletion in Implantable Cardioverter Defibrillators and Cardiac Resynchronization Therapy Defibrillators (CRT'Ds)
2021-03-08BIOTRONIK IncThere is a potential for premature battery depletion in Implantable Cardioverter Defibrillators and Cardiac Resynchronization Therapy Defibrillators (CRT'Ds)
2021-03-08BIOTRONIK IncThere is a potential for premature battery depletion in Implantable Cardioverter Defibrillators and Cardiac Resynchronization Therapy Defibrillators (CRT'Ds)

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.