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