FDA Adverse Event
Malfunction
Summary report: N
9900
MDR report key: 2201286
·
Received August 3, 2011
Report
- Report Number
- 1720753-2011-20656
- Event Type
- Malfunction
- Date Received
- August 3, 2011
- Date of Event
- July 26, 2011
- Report Date
- August 3, 2011
- Manufacturer
- GE OEC MEDICAL SYSTEMS (SLC)
- Product Code
- JAA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- OR, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
A GE SERVICE REP PERFORMED AN ONSITE INVESTIGATION. THE SERVICE REP RESEATED THE CONNECTORS AND ADJUSTED THE VOLTAGE. 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 IN THE LATERAL POSITION, THE SYSTEM WOULD NOT PROVIDE AN IMAGE OR SHUT DOWN AFTER POWERING DOWN. THIS OCCURRED 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 |