9800 Adverse Event — Malfunction (MDR 1720753-2008-16332)
9800 Adverse Event — Malfunction (MDR 1720753-2008-16332) 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 | 1720753-2008-16332 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-21 |
| Report source | Health Professional, User facility |
| Narrative | A GE SVC REP PERFORMED AN ON SITE INVESTIGATION. THE MALFUNCTION WAS VERIFIED. REPLACED THE F1 FUSER ON THE POWER CONTROL PCBA. THE SYS WAS TESTED AND FOUND TO BE WORKING AS INTENDED AND PLACED BACK INTO SVC. |
| Source | openFDA MAUDE (device adverse events) |
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