MalfunctionGBW
CATHETER PUDENZ PERITONEAL LOW PRESSURE STRIPE
Received May 20, 2004
Report 2648988-2004-00020 · MDR key 563041
Device
Generic name
Csf Product
Manufacturer
Integra Neurosciences, Inc.Model number
*Catalog number
NL850-1390
Lot number
*
Product problems
- Tears, rips, holes in device, device material
- Device, removal of (non-implant)
Patient
*
- No Consequences Or Impact To Patient
Narrative
Description of Event or Problem
THE USER FACILITY REPORTED CATHETER WAS IMPLANTED ON A PT WITH A PROGRAMMABLE VALVE SHUNT (V-P SHUNT) SYSTEM IN 1996. SINCE THE PHYSICIAN NOTICED THAT THE CATHETER WAS TORN IN DEC. 2003. THE CATHETER WAS REMOVED IN 2003. NO PT INJURY WAS REPORTED.