FDA Adverse Event
Malfunction
Summary report: N
GE OEC 9800
MDR report key: 1070269
·
Received July 9, 2008
Report
- Report Number
- 1720753-2008-20494
- Event Type
- Malfunction
- Date Received
- July 9, 2008
- Date of Event
- March 28, 2008
- Report Date
- April 7, 2008
- Manufacturer
- GE OEC MEDICAL SYSTEMS INC.
- Product Code
- JAA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MA, US
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
Additional Manufacturer Narrative · 1
A GE REP EVALUATED THE SYSTEM AND REPAIRED THE LEMO CONNECTOR. SYSTEM IS OPERATING AS INTENDED.
Description of Event or Problem · 1
CUSTOMER REPORTED THE SYSTEM IS DISPLAYING A PRE-CHARGE ERROR. NO PT INJURY WAS REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | GE OEC 9800 | FLUOROSCOPIC X-RAY | JAA | GE OEC MEDICAL SYSTEMS INC. | 9800 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |