FDA Adverse Event Summary report: N

AVA HF-ADVANCED VENOUS ACCESS DEVICES

MDR report key: 1889451 · Received October 29, 2010

Report

Report Number
1889451
Date Received
October 29, 2010
Date of Event
October 26, 2010
Report Date
October 29, 2010
Manufacturer
EDWARD LIFESCIENCES LLC
Product Code
DQO
Report Source
User Facility report
Reporter Location
VA, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

PHYSICIAN WAS CHANGING OUT A CENTRAL LINE OVER A WIRE. THEY PASSED THE WIRE THROUGH THE CATHETER AND IT GOT STUCK IN THE SIDE AND ALMOST SNAPPED. ALTHOUGH THIS WAS IN THE PT WHEN THIS HAPPENED THEY WERE ABLE TO GET IT OUT AND THE PT WAS NOT HARMED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 AVA HF-ADVANCED VENOUS ACCESS DEVICES AVA HF-ADVANCED VENOUS ACCESS DEVICES DQO EDWARD LIFESCIENCES LLC * 58749675

Patients

Seq Age Sex Outcome Treatment
1 63 YR