FDA Adverse Event Malfunction Summary report: N

VITALITY AVT FAST-CHARGE

MDR report key: 1041502 · Received May 8, 2008

Report

Report Number
2124215-2008-32031
Event Type
Malfunction
Date Received
May 8, 2008
Date of Event
December 4, 2007
Report Date
February 15, 2008
Manufacturer
CARDIAC PACEMAKERS, INC
Product Code
LWS
Removal / Correction Number
Z47/53-08
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 VITALITY AVT FAST-CHARGE IMPLANTABLE CARDIOVERTER DEFIBRILLATOR LWS CARDIAC PACEMAKERS, INC A155 NA

Patients

Seq Age Sex Outcome Treatment
1 74 YR Other THE DEVICE 4469/435169 WAS IMPLANTED 18-FEB-2005| THE DEVICE 0149/101256 WAS IMPLANTED 18-FEB-2005