FDA Adverse Event
Malfunction
Summary report: N
9800
MDR report key: 2042924
·
Received March 25, 2011
Report
- Report Number
- 1720753-2011-02829
- Event Type
- Malfunction
- Date Received
- March 25, 2011
- Date of Event
- March 1, 2011
- Report Date
- March 25, 2011
- Manufacturer
- GE OEC MEDICAL SYSTEMS (SLC)
- Product Code
- JAA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NV, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
A GE SERVICE REPRESENTATIVE PERFORMED AN ON SITE INVESTIGATION. THE ENGINEER FOUND THE C-ARM CABLE HAD BEEN REPLACED WITH A NON HOSPITAL GRADE PLUG. THE POWER CABLE ASSEMBLY WAS REPLACED. THE SYSTEM WAS THEN FOUND TO BE OPERATING AS INTENDED.
Description of Event or Problem · 1
THE CUSTOMER REPORTED THE SYSTEMS' POWER PLUG HAD EXPOSED WIRES. NO REPORT OF PATIENT INJURY.
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 |