FDA Adverse Event
Malfunction
Summary report: N
2800
MDR report key: 3860441
·
Received April 15, 2014
Report
- Report Number
- 1720753-2014-03295
- Event Type
- Malfunction
- Date Received
- April 15, 2014
- Date of Event
- March 24, 2014
- Report Date
- April 15, 2014
- Manufacturer
- GE OEC MEDICAL SYSTEMS (SLC)
- Product Code
- JAA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- WV, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
A GE SERVICE REP PERFORMED AN ONSITE INVESTIGATION. THE COLLIMATOR INTERFACE AND PS4 POWER SUPPLY WERE EVALUATED AND REPLACED. THE SYSTEM WAS TESTED AND FOUND TO WORKING AS INTENDED AND RETURNED TO SERVICE.
Description of Event or Problem · 1
THE CUSTOMER REPORTED THAT THE SYSTEM REPEATEDLY LOCKED UP. NO PT SERIOUS INJURY OR DEATH WAS REPORTED RELATED TO THIS EVENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 230548 | 2800 | FLUOROSCOPIC X-RAY | JAA | GE OEC MEDICAL SYSTEMS (SLC) | 2800 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |