FDA Adverse Event
Malfunction
Summary report: N
9800
MDR report key: 2081952
·
Received April 5, 2011
Report
- Report Number
- 1720753-2011-03252
- Event Type
- Malfunction
- Date Received
- April 5, 2011
- Date of Event
- March 18, 2011
- Report Date
- April 5, 2011
- Manufacturer
- GE OEC MEDICAL SYSTEMS (SLC)
- Product Code
- JAA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FL, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE MANUFACTURER'S SERVICE REPRESENTATIVE PERFORMED AN ON-SITE INVESTIGATION. THE BATTERY PACK WAS REPLACED AND THE FILAMENT WAS CALIBRATED. THE SYSTEM WAS TESTED AND OPERATES AS INTENDED. THIS EVENT COULD BE A POSSIBLE ACCIDENTAL RADIATION OCCURRENCE.
Description of Event or Problem · 1
THE CUSTOMER REPORTED THAT THE 9800 SYSTEM DISPLAYED A HIGH MILLIAMP ERROR MESSAGE. NO PATIENT INJURY WAS REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | 9800 | FLUOROSCOPIC X-RAY | JAA | GE OEC MEDICAL SYSTEMS (SLC) | 9800 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |