FDA Adverse Event
Injury
Summary report: N
CYBERONICS NEUROCYBERNETIC PROSTHESIS
MDR report key: 318146
·
Received February 23, 2001
Report
- Report Number
- 1644487-2001-00101
- Event Type
- Injury
- Date Received
- February 23, 2001
- Date of Event
- July 14, 2000
- Report Date
- July 17, 2000
- Manufacturer
- CYBERONICS, INC.
- Product Code
- LYJ
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Occupation
- PATIENT FAMILY MEMBER OR FRIEND
Narratives
Description of Event or Problem · 1
DESCRIBE EVENT OR PROBLEM: INFECTION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 7465 | CYBERONICS NEUROCYBERNETIC PROSTHESIS | NEUROSTIMULATOR | LYJ | CYBERONICS, INC. | 101 | 37488C |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 46 YR | Hospitalization| R | MODEL 300-20 BIPOLAR LEAD,| EXPIRE 3/1/2002, DATE OF MFG 3/2000,| STERILIZATION LOT# 36465C. |