FDA Adverse Event Malfunction Summary report: N

SETROX S 45

MDR report key: 2091336 · Received May 4, 2011

Report

Report Number
1028232-2011-01006
Event Type
Malfunction
Date Received
May 4, 2011
Date of Event
March 28, 2011
Report Date
April 27, 2011
Manufacturer
BIOTRONIK SE & CO. KG
Product Code
NVZ
PMA / PMN Number
P950037
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OR, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

THIS LEAD WAS EXPLANTED DUE TO A POSSIBLE BREAK IN THE LEAD BODY CLOSE TO THE PIN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SETROX S 45 PACER LEAD NVZ BIOTRONIK SE & CO. KG 350973

Patients

Seq Age Sex Outcome Treatment
1 75 YR Hospitalization