FDA Adverse Event
Injury
Summary report: N
CYBERONICS NEUROCYBERNETIC PROSTHESIS
MDR report key: 317982
·
Received February 23, 2001
Report
- Report Number
- 1644487-2001-00117
- Event Type
- Injury
- Date Received
- February 23, 2001
- Date of Event
- September 16, 2000
- Report Date
- October 6, 2000
- Manufacturer
- CYBERONICS, INC.
- Product Code
- LYJ
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TN, US
- Reporter Occupation
- PHYSICIAN
Narratives
Description of Event or Problem · 1
DESCRIBE EVENT OR PROBLEM: INFECTION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 7217 | CYBERONICS NEUROCYBERNETIC PROSTHESIS | NEUROSTIMULATOR | LYJ | CYBERONICS, INC. | 101 | 38008C |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 10 YR | Hospitalization| O | MODEL 300-20 BIPOLAR LEAD,| STERILIZATION LOT# 38588C.| EXPIRE 05/2002, DATE OF MFG 05/2000, |