CAPSURE FIX MRI Adverse Event — Malfunction (MDR 2649622-2020-08378)
CAPSURE FIX MRI Adverse Event — Malfunction (MDR 2649622-2020-08378) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CAPSURE FIX MRI; Generic name: DRUG ELUTING PERMANENT RIGHT VENTRICULAR (RV) OR RIGHT ATRIA; Manufacturer: MPRI.
| Device | CAPSURE FIX MRI |
|---|---|
| Generic name | DRUG ELUTING PERMANENT RIGHT VENTRICULAR (RV) OR RIGHT ATRIA |
| Manufacturer | MPRI |
| Report number | 2649622-2020-08378 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | CONSUMER |
| Narrative | CONCOMITANT MEDICAL PRODUCTS: 97702 PAIN STIM IPG IMPLANT DATE: (B)(6) 2018; 977C165 PAIN STIM LEAD IMPLANT DATE: (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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