COGNIS Adverse Event — Malfunction (MDR 2124215-2020-09244)
COGNIS Adverse Event — Malfunction (MDR 2124215-2020-09244) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: COGNIS; Generic name: IMPLANTABLE PULSE GENERATOR, PACEMAKER (NON-CRT); Manufacturer: BOSTON SCIENTIFIC CORPORATION.
| Device | COGNIS |
|---|---|
| Generic name | IMPLANTABLE PULSE GENERATOR, PACEMAKER (NON-CRT) |
| Manufacturer | BOSTON SCIENTIFIC CORPORATION |
| Report number | 2124215-2020-09244 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE |
| Narrative | THIS SUPPLEMENTAL REPORT IS BEING FILED DUE TO THE COMPLETED EVALUATION OF THIS PRODUCT. |
| Source | openFDA MAUDE (device adverse events) |
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