FDA Adverse Event Other Summary report: N

MEDTRONICS SOFAMOR DANEK

MDR report key: 538778 · Received August 12, 2004

Report

Report Number
538778
Event Type
Other
Date Received
August 12, 2004
Date of Event
June 22, 2004
Report Date
August 11, 2004
Manufacturer
MEDTRONICS
Product Code
JXG
Product Problem
Yes
Report Source
User Facility report
Reporter Location
FL, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

VP SHUNT REVISION DUE TO MALFUNCTIONING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MEDTRONICS SOFAMOR DANEK SNAP SHUNT CATHETER STANDARD JXG MEDTRONICS * 34668
2 MEDTRONIC SOFAMOR DANEK STRATA SNAP SHUNT ASSEMBLY 120 CM REGULAR JXG MEDTRONICS * 22139

Patients

Seq Age Sex Outcome Treatment
1 79 YR Other