DACRON GRAFT Adverse Event — Injury (MDR 1000274)
DACRON GRAFT Adverse Event — Injury (MDR 1000274) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: DACRON GRAFT; Generic name: DACRON GRAFT; Manufacturer: DATASCOPE INTERVASCULAR, INC..
| Device | DACRON GRAFT |
|---|---|
| Generic name | DACRON GRAFT |
| Manufacturer | DATASCOPE INTERVASCULAR, INC. |
| Report number | 1000274 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2008-01-16 |
| Narrative | THE PATIENT RECEIVED AN AORTIC ROOT REPLACEMENT AND REIMPLANTATION OF CORONARY ARTERIES WITH MEDTRONIC FREESTYLE PROCINE AORTIC ROOT VALVE REPLACEMENT AND DATASCOPE INTERVASCULAR DACRON EXTENSION GRAFT. THE PATIENT WAS READMITTED 8 MONTHS LATER (FOR 31 DAYS TOTAL ADMISSION) WITH A THREE WEEK HISTORY OF FEVERS. PATIENT HAD PREVIOUS ADMISSIONS TO A HOSPITAL IN ANOTHER COUNTRY PRIOR TO THE CURRENT AD |
| Source | openFDA MAUDE (device adverse events) |
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