FDA Adverse Event
Malfunction
Summary report: N
8800
MDR report key: 2102124
·
Received April 20, 2011
Report
- Report Number
- 9617766-2011-00921
- Event Type
- Malfunction
- Date Received
- April 20, 2011
- Date of Event
- April 13, 2011
- Report Date
- April 20, 2011
- Manufacturer
- GE MEDICAL SYSTEMS (INDIA) PRIVATE, LTD. (GE PRIVATE)
- Product Code
- JAA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- PA, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE MFR'S SERVICE REP PERFORMED AN ON-SITE INVESTIGATION. THE BATTERIES WERE REPLACED, AND THE FILAMENT WAS CALIBRATED. THE SYSTEM WAS TESTED AND IS OPERATING AS INTENDED.
Description of Event or Problem · 1
THE CUSTOMER REPORTED THAT THE 8800 SYSTEM DISPLAYED AN ERROR MESSAGE UPON BOOT UP. NO PT INJURY WAS REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | 8800 | FLUOROSCOPIC X-RAY | JAA | GE MEDICAL SYSTEMS (INDIA) PRIVATE, LTD. (GE PRIVATE) | 8800 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |