FDA Adverse Event
Injury
Summary report: N
CYBERONICS NEUROCYBERNETIC PROSTHESIS
MDR report key: 318407
·
Received February 23, 2001
Report
- Report Number
- 1644487-2001-00026
- Event Type
- Injury
- Date Received
- February 23, 2001
- Date of Event
- May 14, 1998
- Report Date
- May 19, 1998
- Manufacturer
- CYBERONICS, INC.
- Product Code
- LYJ
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IN, US
- Reporter Occupation
- PHYSICIAN
Narratives
Description of Event or Problem · 1
INFECTION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 7236 | CYBERONICS NEUROCYBERNETIC PROSTHESIS | NEUROSTIMULATOR | LYJ | CYBERONICS, INC. | 100 | 7062C |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 9 YR | Hospitalization| O| R | BIPOLAR LEAD 300-20-6021.| STERILIZATION LOT# 6850C.| EXPIRE 01/26/2000, DATE OF MFG 1/22/1998 |