FDA Adverse Event Injury Summary report: N

BARD PORT WITH OPEN ENDED CATH

MDR report key: 425384 · Received October 22, 2002

Report

Report Number
425384
Event Type
Injury
Date Received
October 22, 2002
Date of Event
October 10, 2002
Report Date
October 22, 2002
Manufacturer
BARD
Product Code
LJT
Adverse Event
Yes
Product Problem
Yes
Report Source
User Facility report
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

NOTED INFUSAPORT NOT FUNCTIONING, LEAKING OF FLUID INTO SURROUNDING TISSUE. LAST USE OF PORT WAS 10/03/2002 WITH NO PROBLEM. X-RAY REVEALED TUBING SHEARED OFF AT LEVEL OF CLAVICLE AND TRAVELLED TO RIGHT PULMONARY ARTERY. PORT AND TUBING REMOVED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BARD PORT WITH OPEN ENDED CATH IMPLANTABLE PORT LJT BARD * *

Patients

Seq Age Sex Outcome Treatment
1 55 YR Hospitalization| R