FDA Adverse Event
Malfunction
Summary report: N
9900
MDR report key: 2201288
·
Received August 3, 2011
Report
- Report Number
- 1720753-2011-20653
- Event Type
- Malfunction
- Date Received
- August 3, 2011
- Date of Event
- July 19, 2011
- Report Date
- August 3, 2011
- Manufacturer
- GE OEC MEDICAL SYSTEMS (SLC)
- Product Code
- JAA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- GA, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
A GE SERVICE REPRESENTATIVE PERFORMED AN ON SITE INVESTIGATION. THE SERVICE REP REPLACED THE X-RAY TUBE, PERFORMED A FILAMENT CALIBRATION, REGREASED THE HIGH VOLTAGE CABLE STICKS AND PERFORMED A HIGH VOLTAGE ARC TEST. THE SYSTEM WAS TESTED AND FOUND TO BE WORKING AS INTENDED AND PUT BACK IN SERVICE.
Description of Event or Problem · 1
THE CUSTOMER REPORTED THAT THE SYSTEM ARCED INTERMITTENTLY. THIS HAPPENED DURING A PROCEDURE. NO PT INJURY WAS REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | 9900 | FLUOROSCOPIC X-RAY | JAA | GE OEC MEDICAL SYSTEMS (SLC) | 9900 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |