FDA Adverse Event
Malfunction
Summary report: N
9800
MDR report key: 3101692
·
Received April 30, 2013
Report
- Report Number
- 1720753-2013-05475
- Event Type
- Malfunction
- Date Received
- April 30, 2013
- Date of Event
- April 9, 2013
- Report Date
- April 30, 2013
- Manufacturer
- GE OEC MEDICAL SYSTEMS (SLC)
- Product Code
- JAA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- EZ
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
A GE SERVICE REPRESENTATIVE PERFORMED AN ON SITE INVESTIGATION. THE BATTERIES WERE IDENTIFIED AS BEING FAULTY. A REPAIR QUOTE WAS ISSUED TO THE CUSTOMER AND IS PENDING APPROVAL.
Description of Event or Problem · 1
THE CUSTOMER REPORTED THAT THE SYSTEM DISPLAYED A PRECHARGE ERROR MESSAGE. THIS ERROR MESSAGE WILL LIKELY PREVENT THE SYSTEM FROM BOOTING UP. THERE IS NO REPORT OF PT INJURY ASSOCIATED WITH THIS EVENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 187656 | 9800 | FLUOROSCOPIC X-RAY | JAA | GE OEC MEDICAL SYSTEMS (SLC) | 9800 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |