FDA Adverse Event Malfunction Summary report: N

GUARDIAN II NC HEMOSTASIS VALVE

MDR report key: 2994429 · Received March 8, 2013

Report

Report Number
3005395947-2013-00006
Event Type
Malfunction
Date Received
March 8, 2013
Date of Event
January 4, 2013
Report Date
March 8, 2013
Manufacturer
VASCULAR SOLUTIONS ZERUSA LIMITED
Product Code
DTL
PMA / PMN Number
K122301
Removal / Correction Number
3005395947-02/28/2013-01
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MO, US
Reporter Occupation
PHYSICIAN

Narratives

Description of Event or Problem · 1

USER-FACILITY REPORTED PHYSICIANS EXPERIENCING INTRODUCTION OF AIR WHILE USING THE GUARDIAN II NC HEMOSTASIS VALVE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
99715 GUARDIAN II NC HEMOSTASIS VALVE HEMOSTASIS VALVE DTL VASCULAR SOLUTIONS ZERUSA LIMITED 8216 25615

Patients

Seq Age Sex Outcome Treatment
1 Life Threatening