FDA Adverse Event
Malfunction
Summary report: N
8800
MDR report key: 2081907
·
Received April 5, 2011
Report
- Report Number
- 9617766-2011-00798
- Event Type
- Malfunction
- Date Received
- April 5, 2011
- Date of Event
- February 22, 2011
- Report Date
- April 5, 2011
- Manufacturer
- GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD (GE PRIVATE)
- Product Code
- JAA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- GM
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
A GE SERVICE REP PERFORMED AN ON-SITE INVESTIGATION. ELECTRICAL TESTS WERE PERFORMED. THE INTERCONNECT CABLE AND THE LEMO SOCKET WERE REPLACED. THE SYSTEM WAS TESTED AND OPERATES AS INTENDED.
Description of Event or Problem · 1
THE CUSTOMER REPORTED THE IMAGES ON THE 8800 SYSTEM TRAVELED ON EACH MONITOR. 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 |