FDA Adverse Event
Injury
Summary report: N
HAKIM VALVE
MDR report key: 297149
·
Received September 20, 2000
Report
- Report Number
- 9612007-2000-00037
- Event Type
- Injury
- Date Received
- September 20, 2000
- Date of Event
- June 29, 2000
- Report Date
- September 18, 2000
- Manufacturer
- NMT NEUROSCIENCES IMPLANTS S.A.
- Product Code
- JXG
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NZ
- Reporter Occupation
- PHYSICIAN
Narratives
Description of Event or Problem · 1
POST IMPLANTATION, PT EXPERIENCED HEADACHES, NAUSEA AND VOMITING.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | HAKIM VALVE | HYDROCEPHALUS VALVE | JXG | NMT NEUROSCIENCES IMPLANTS S.A. | NA | 104195 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 50 YR | Required Intervention |