FDA Adverse Event
Malfunction
Summary report: N
8800
MDR report key: 1220633
·
Received October 31, 2008
Report
- Report Number
- 9617766-2008-01395
- Event Type
- Malfunction
- Date Received
- October 31, 2008
- Date of Event
- October 10, 2008
- Report Date
- October 28, 2008
- Manufacturer
- GE OEC MEDICAL SYSTEMS INC.
- Product Code
- JAA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- JA
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
Additional Manufacturer Narrative · 1
THE GE SERVICE REP REPLACED THE POWER SUPPLY.
Description of Event or Problem · 1
THE CUSTOMER REPORTED THE VERTICAL COLUMN INTERMITTENTLY DID NOT MOVE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | 8800 | FLUOROSCOPIC X-RAY | JAA | GE OEC MEDICAL SYSTEMS INC. | NA | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |