FDA Adverse Event
Malfunction
Summary report: N
GE OEC 2600
MDR report key: 2998033
·
Received February 15, 2008
Report
- Report Number
- 1720753-2008-29626
- Event Type
- Malfunction
- Date Received
- February 15, 2008
- Date of Event
- February 7, 2008
- Report Date
- February 14, 2008
- Manufacturer
- GE OEC MEDICAL SYSTEMS INC
- Product Code
- JAA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FL, US
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
Additional Manufacturer Narrative · 1
A GE REP EVALUATED THE SYSTEM AND FOUND A CABLE HARNESS INTERFERING WITH LATERAL MOVEMENT. GE REP REPAIRED THE SYSTEM, SYSTEM OPERATES AS INTENDED.
Description of Event or Problem · 1
THE CUSTOMER REPORTED A LATERAL TACKLE ERROR IS BEING DISPLAYED. NO PT INJURY WAS REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | GE OEC 2600 | FLUOROSCOPIC X-RAY | JAA | GE OEC MEDICAL SYSTEMS INC | 2600 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |