9800 Adverse Event — Malfunction (MDR 1720753-2008-16326)
9800 Adverse Event — Malfunction (MDR 1720753-2008-16326) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: 9800; Generic name: FLUOROSCOPIC X-RAY; Manufacturer: GE OEC MEDICAL SYSTEMS, INC.
| Device | 9800 |
|---|---|
| Generic name | FLUOROSCOPIC X-RAY |
| Manufacturer | GE OEC MEDICAL SYSTEMS, INC |
| Report number | 1720753-2008-16326 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-21 |
| Report source | Health Professional, User facility |
| Narrative | IT WAS REPORTED THAT THE LEFT MONITOR ON THE 9800 SYS IS GOING DARK DURING CASES. IT WAS NOTED THAT THE IMAGES RECALLED FROM THE HARD DRIVE LOOK GOOD. THERE WAS NO REPORT OF PT INJURY. |
| Source | openFDA MAUDE (device adverse events) |
🔍 Search all device adverse events →
$1999/mo
Try DeviceEvents →