FDA Adverse Event
Malfunction
Summary report: N
9900
MDR report key: 2102721
·
Received May 23, 2011
Report
- Report Number
- 1720753-2011-07536
- Event Type
- Malfunction
- Date Received
- May 23, 2011
- Date of Event
- May 13, 2011
- Report Date
- May 23, 2011
- Manufacturer
- GE OEC MEDICAL SYSTEMS (SLC)
- Product Code
- JAA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- VA, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
A GE SERVICE REPRESENTATIVE PERFORMED AN ONSITE INVESTIGATION. THE INTELLIGENT SHUT DOWN DEVICE JUMPER WAS MOVED TO THE AC MONITOR BECAUSE OF THE LOW/HIGH ALARMS REPORTED BY THE CUSTOMER. THE SYSTEM WAS TESTED AND FOUND TO BE WORKING AS INTENDED AND PUT BACK INTO SERVICE.
Description of Event or Problem · 1
THE CUSTOMER REPORTED THAT DURING A PROCEDURE THE SYSTEM WOULD NOT POWER ON AND WAS PRODUCING A HIGH POWER ALARM WHEN IT WAS PLUGGED IN. NO PATIENT INJURY WAS REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | 9900 | FLUOROSCOPIC X-RAY | JAA | GE OEC MEDICAL SYSTEMS (SLC) | 9900 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |