9800 Adverse Event — Malfunction (MDR 1720753-2008-16330)
9800 Adverse Event — Malfunction (MDR 1720753-2008-16330) 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 | 1720753-2008-16330 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-21 |
| Report source | Health Professional, User facility |
| Narrative | IT WAS REPORTED THAT THE C-ARM ON THE 9800 SYS IS NOT GOING UP. THEY ARE STILL USING THE SYS. THERE WAS NO REPORT OF PT INJURY. |
| Source | openFDA MAUDE (device adverse events) |
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