FDA Adverse Event Injury Summary report: N

CAPSURE Z NOVUS

MDR report key: 632792 · Received January 10, 2005

Report

Report Number
2649622-2005-00046
Event Type
Injury
Date Received
January 10, 2005
Date of Event
October 18, 2004
Manufacturer
MEDTRONIC PUERTO RICO, INC.
Product Code
DXY
Removal / Correction Number
NI
Report Source
Manufacturer report
Reporter Location
IL
Reporter Occupation
INVALID DATA

Narratives

Description of Event or Problem · 1

PACING WASN'T FUNCTIONAL POST-AVJ ABLATION AND HIGH IMPEDANCE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CAPSURE Z NOVUS IMPLANTABLE PACING LEAD DXY MEDTRONIC PUERTO RICO, INC. 5054 NA

Patients

Seq Age Sex Outcome Treatment
1 000 Other