FDA Adverse Event Other Summary report: N

NEOSTAR CENTRAL VENOUS CATHETER

MDR report key: 2484822 · Received March 6, 2012

Report

Report Number
1056436-2012-00022
Event Type
Other
Date Received
March 6, 2012
Date of Event
February 24, 2012
Report Date
March 6, 2012
Manufacturer
ANGIODYNAMICS
Product Code
DQO
PMA / PMN Number
NA
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Description of Event or Problem · 1

MICRO PUNCTURES/HOLES IN THE HUB EXTENSIONS OF THE VENUS AND ARTERIAL LUMENS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 NEOSTAR CENTRAL VENOUS CATHETER CHRONIC CVC CATHETER DQO ANGIODYNAMICS NA 554416

Patients

Seq Age Sex Outcome Treatment
1