2800 Adverse Event — Malfunction (MDR 1720753-2008-16321)
2800 Adverse Event — Malfunction (MDR 1720753-2008-16321) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: 2800; Generic name: FLUOROSCOPIC X-RAY; Manufacturer: GE OEC MEDICAL SYSTEMS, INC.
| Device | 2800 |
|---|---|
| Generic name | FLUOROSCOPIC X-RAY |
| Manufacturer | GE OEC MEDICAL SYSTEMS, INC |
| Report number | 1720753-2008-16321 |
| 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. SECURED A LOOSE CONNECTOR IN THE TUBE HEAD. 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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