FDA Adverse Event Malfunction Summary report: N

MEDCOMP PD CATH

MDR report key: 853065 · Received May 14, 2007

Report

Report Number
MW1042878
Event Type
Malfunction
Date Received
May 14, 2007
Date of Event
May 14, 2007
Report Date
May 14, 2007
Manufacturer
MPS MEDICAL PRODUCT SERVICE GMBH
Product Code
LFK
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
FL, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

PERITONEAL CATHETER TUNNELER BROKE OFF.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MEDCOMP PD CATH PERITONEAL DIALYSIS CATHETER KIT WITH TWO CUFFS LFK MPS MEDICAL PRODUCT SERVICE GMBH MPD-257 MAGN880

Patients

Seq Age Sex Outcome Treatment
1 59 YR