9900 Adverse Event — Malfunction (MDR 1720753-2008-16309)
9900 Adverse Event — Malfunction (MDR 1720753-2008-16309) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: 9900; Generic name: FLUOROSCOPIC X-RAY; Manufacturer: GE OEC MEDICAL SYSTEMS INC..
| Device | 9900 |
|---|---|
| Generic name | FLUOROSCOPIC X-RAY |
| Manufacturer | GE OEC MEDICAL SYSTEMS INC. |
| Report number | 1720753-2008-16309 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-21 |
| Report source | Health Professional, User facility |
| Narrative | IT WAS REPORTED THAT THE 9900 SYSTEM IS COMPLETELY DOWN. CASE MOVED TO ANOTHER SYSTEM. THERE WAS NO REPORT OF PATIENT INJURY. |
| Source | openFDA MAUDE (device adverse events) |
🔍 Search all device adverse events →
$1999/mo
Try DeviceEvents →