FDA Adverse Event
Other
Summary report: N
MEDTRONIC
MDR report key: 561434
·
Received January 13, 2004
Report
- Report Number
- 561434
- Event Type
- Other
- Date Received
- January 13, 2004
- Date of Event
- November 14, 2003
- Report Date
- January 13, 2004
- Manufacturer
- MEDTRONIC NEUROLOGICAL
- Product Code
- GZB
- Report Source
- User Facility report
- Reporter Location
- IL, US
Narratives
Description of Event or Problem · 1
THE PATIENT CAME TO THE OR FOR REMOVAL OF SPINAL CORD STIMLATOR THAT WAS INFECTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | MEDTRONIC | SPINAL CORD STIMULATOR | GZB | MEDTRONIC NEUROLOGICAL | ITREL3 | 742 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 53 YR |