FDA Adverse Event
Malfunction
Summary report: N
STENOSCOP
MDR report key: 2153500
·
Received June 21, 2011
Report
- Report Number
- 9617766-2011-01268
- Event Type
- Malfunction
- Date Received
- June 21, 2011
- Date of Event
- June 10, 2011
- Report Date
- June 21, 2011
- Manufacturer
- GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD.
- Product Code
- JAA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FR
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
A GE SERVICE REPRESENTATIVE PERFORMED AN ONSITE INVESTIGATION, AND REPAIRED A FUSE. 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 BOTH MONITORS ON THE SYSTEM WOULD NOT DISPLAY AN IMAGE. NO PATIENT INJURY WAS REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | STENOSCOP | FLUOROSCOPIC X-RAY | JAA | GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD. | STENOSCOP |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |