FDA Adverse Event
Malfunction
Summary report: N
9800
MDR report key: 2030586
·
Received March 9, 2011
Report
- Report Number
- 1720753-2011-02096
- Event Type
- Malfunction
- Date Received
- March 9, 2011
- Date of Event
- February 20, 2011
- Report Date
- March 9, 2011
- Manufacturer
- GE OEC MEDICAL SYSTEMS (SLC)
- Product Code
- JAA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- AS
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
A GE REPRESENTATIVE EVALUATED THE SYSTEM AND REPLACED THE VIDEO CONTROL BOARD, HIGH VOLTAGE POWER SUPPLY REGULATOR, AND BACKPLANE, AND PERFORMED A FILAMENT CALIBRATION. THE SYSTEM OPERATES AS INTENDED.
Description of Event or Problem · 1
THE CUSTOMER REPORTED THE IMAGE TURNED BLACK AND STARTED TO FLICKER, AND THE SYSTEM DISPLAYED AN MA SENSOR ERROR. NO PATIENT INJURY WAS REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | 9800 | FLUOROSCOPIC X-RAY | JAA | GE OEC MEDICAL SYSTEMS (SLC) | 9800 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |