FDA Adverse Event Malfunction Summary report: N

LIFE PORT

MDR report key: 34838 · Received July 31, 1996

Report

Report Number
MW1009604
Event Type
Malfunction
Date Received
July 31, 1996
Date of Event
March 27, 1996
Report Date
March 29, 1996
Manufacturer
STRATO INFUSAID, INC.
Product Code
LJT
Product Problem
Yes
Report Source
Voluntary report
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

TUBING FOUND TO BE DISCONNECTED FROM PORT ITSELF. PORT PLACED 6/6/95 FOR CHEMO ADMINISTRATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 LIFE PORT IMPLANTABLE PORT LJT STRATO INFUSAID, INC. 12456

Patients

Seq Age Sex Outcome Treatment
1 NO INFO