7700 Adverse Event — Malfunction (MDR 9680959-2008-00025)
7700 Adverse Event — Malfunction (MDR 9680959-2008-00025) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: 7700; Generic name: FLUOROSCOPIC X-RAY; Manufacturer: GE OEC MEDICAL SYSTEMS INC..
| Device | 7700 |
|---|---|
| Generic name | FLUOROSCOPIC X-RAY |
| Manufacturer | GE OEC MEDICAL SYSTEMS INC. |
| Report number | 9680959-2008-00025 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-20 |
| Report source | Health Professional, User facility |
| Narrative | A GE SERVICE REP PERFORMED AN ON SITE INVESTIGATION. ORDERED AND DELIVERED A REPLACEMENT IMAGE INTENSIFIER (II) POWER SUPPLY TO CUSTOMER. IT IS BELIEVED THAT THIS COMPONENT WILL ADDRESS THE REPORTED ISSUE. NO ADDITIONAL INFO AT THIS TIME. IF ADDITIONAL INFO IS RECEIVED THAT INDICATES, OTHERWISE AN ADDITIONAL REPORT WILL BE FILED AS REQUIRED. |
| Source | openFDA MAUDE (device adverse events) |
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