PERCEPTA QUAD CRT-P MRI SURESCAN Adverse Event — Malfunction (MDR 3004209178-2020-07808)
PERCEPTA QUAD CRT-P MRI SURESCAN Adverse Event — Malfunction (MDR 3004209178-2020-07808) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PERCEPTA QUAD CRT-P MRI SURESCAN; Generic name: PULSE GENERATOR, PACEMAKER, IMPLANTABLE, WITH CARDIAC RESYNC; Manufacturer: MEDTRONIC PUERTO R
| Device | PERCEPTA QUAD CRT-P MRI SURESCAN |
|---|---|
| Generic name | PULSE GENERATOR, PACEMAKER, IMPLANTABLE, WITH CARDIAC RESYNC |
| Manufacturer | MEDTRONIC PUERTO RICO OPERATIONS CO. |
| Report number | 3004209178-2020-07808 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | HEALTH PROFESSIONAL |
| Narrative | CONCOMITANT MEDICAL PRODUCTS: 429888, LEAD, IMPLANTED: (B)(6) 2018; 5867AS, ADAPTOR, IMPLANTED: (B)(6) 2018. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED. |
| Source | openFDA MAUDE (device adverse events) |
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