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CPR4
MICROPORT CRM SRL · Model B10031 · UDI-DI 08031527019611
MRM
Prescription
0
510(k) clearances
7,873
Adverse events (191 deaths)
34
Recalls
6
Facilities
Description
Inductive Telemetry Head CPR4 USB
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2021-03-08 | BIOTRONIK Inc | There is a potential for premature battery depletion in Implantable Cardioverter Defibrillators and Cardiac Resynchronization Therapy Defibrillators (CRT'Ds) |
| 2021-03-08 | BIOTRONIK Inc | There is a potential for premature battery depletion in Implantable Cardioverter Defibrillators and Cardiac Resynchronization Therapy Defibrillators (CRT'Ds) |
| 2021-03-08 | BIOTRONIK Inc | There is a potential for premature battery depletion in Implantable Cardioverter Defibrillators and Cardiac Resynchronization Therapy Defibrillators (CRT'Ds) |
| 2021-03-08 | BIOTRONIK Inc | There is a potential for premature battery depletion in Implantable Cardioverter Defibrillators and Cardiac Resynchronization Therapy Defibrillators (CRT'Ds) |
| 2021-03-08 | BIOTRONIK Inc | There is a potential for premature battery depletion in Implantable Cardioverter Defibrillators and Cardiac Resynchronization Therapy Defibrillators (CRT'Ds) |
| 2021-03-08 | BIOTRONIK Inc | There is a potential for premature battery depletion in Implantable Cardioverter Defibrillators and Cardiac Resynchronization Therapy Defibrillators (CRT'Ds) |
| 2021-03-08 | BIOTRONIK Inc | There is a potential for premature battery depletion in Implantable Cardioverter Defibrillators and Cardiac Resynchronization Therapy Defibrillators (CRT'Ds) |
| 2021-03-08 | BIOTRONIK Inc | There is a potential for premature battery depletion in Implantable Cardioverter Defibrillators and Cardiac Resynchronization Therapy Defibrillators (CRT'Ds) |
| 2021-03-08 | BIOTRONIK Inc | There is a potential for premature battery depletion in Implantable Cardioverter Defibrillators and Cardiac Resynchronization Therapy Defibrillators (CRT'Ds) |
| 2021-03-08 | BIOTRONIK Inc | There is a potential for premature battery depletion in Implantable Cardioverter Defibrillators and Cardiac Resynchronization Therapy Defibrillators (CRT'Ds) |
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Get your free API keyRead the docsData 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.