FDA Adverse Event Malfunction Summary report: N

V CATH PICC

MDR report key: 67123 · Received February 6, 1997

Report

Report Number
MW1010669
Event Type
Malfunction
Date Received
February 6, 1997
Date of Event
January 27, 1997
Report Date
January 28, 1997
Manufacturer
HDC
Product Code
DQO
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
WA, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

INJECTION OF CT CONTRAST VIA PRESSURE INFUSER CAUSED RUPTURE OF DISTAL (BLUE) LUMEN AT CATHETER - WHITE HUB MOLDING JUNCTION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 V CATH PICC PERIPHERALLY INSERTED CATHETER DQO HDC 395-50 1021

Patients

Seq Age Sex Outcome Treatment
1 79 YR Other