FDA Adverse Event Malfunction Summary report: N

24 GAUGE L CATH PEEL AWAY SYSTEM

MDR report key: 1010497 · Received February 13, 2008

Report

Report Number
1010497
Event Type
Malfunction
Date Received
February 13, 2008
Date of Event
January 22, 2008
Report Date
February 13, 2008
Manufacturer
BECTON DICKINSON INFUSION THERAPY SYSTEMS
Product Code
LJS
Product Problem
Yes
Report Source
User Facility report
Reporter Location
IA, US

Narratives

Description of Event or Problem · 1

NEWLY INSERTED PICC LINE DISLODGED WHEN IT WAS BEING REPOSITIONED. SEVEN CM OF THE CATHETER REMAINED INSIDE THE PATIENT REQUIRING SURGICAL RETRIEVAL AND THE NEED FOR A CENTRAL LINE TO BE PLACED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 24 GAUGE L CATH PEEL AWAY SYSTEM CATHETER, PICC LJS BECTON DICKINSON INFUSION THERAPY SYSTEMS * 7039277

Patients

Seq Age Sex Outcome Treatment
1 18 DA