FDA Adverse Event
Malfunction
Summary report: N
2600
MDR report key: 2023056
·
Received February 24, 2011
Report
- Report Number
- 1720753-2011-01605
- Event Type
- Malfunction
- Date Received
- February 24, 2011
- Date of Event
- February 1, 2011
- Report Date
- February 24, 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 MFR'S SERVICE REP PERFORMED AN ONSITE INVESTIGATION. THE REP RESEATED ALL PCB'S IN THE WORKSTATION. THE SYSTEM WAS TESTED AND OPERATED AS INTENDED.
Description of Event or Problem · 1
THE CUSTOMER REPORTED, THE 2600 SYSTEM NEEDS TO BE REBOOTED MULTIPLE TIMES TO TAKE IMAGES. NO PT INJURY WAS REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | 2600 | FLUOROSCOPIC X-RAY | JAA | GE OEC MEDICAL SYSTEMS (SLC) | 2600 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |