PERCEPTA CRT-P MRI SURESCAN Adverse Event — Malfunction (MDR 3004209178-2020-07757)
PERCEPTA CRT-P MRI SURESCAN Adverse Event — Malfunction (MDR 3004209178-2020-07757) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PERCEPTA CRT-P MRI SURESCAN; Generic name: PULSE GENERATOR, PACEMAKER, IMPLANTABLE, WITH CARDIAC RESYNC; Manufacturer: MEDTRONIC PUERTO RICO OPERAT
| Device | PERCEPTA CRT-P MRI SURESCAN |
|---|---|
| Generic name | PULSE GENERATOR, PACEMAKER, IMPLANTABLE, WITH CARDIAC RESYNC |
| Manufacturer | MEDTRONIC PUERTO RICO OPERATIONS CO. |
| Report number | 3004209178-2020-07757 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | HEALTH PROFESSIONAL |
| Narrative | PRODUCT EVENT SUMMARY: THE DEVICE WAS NOT RETURNED FOR ANALYSIS, HOWEVER, PERFORMANCE DATA COLLECTED FROM THE DEVICE WAS RECEIVED AND ANALYZED. ANALYSIS OF THE DEVICE MEMORY HAD AN OBSERVATION RELATING TO THE BATTERY LONGEVITY ESTIMATOR. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED. |
| Source | openFDA MAUDE (device adverse events) |
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