FDA Adverse Event Malfunction Summary report: N

MERLIN PROGRAMMER

MDR report key: 2905003 · Received January 9, 2013

Report

Report Number
2017865-2013-00789
Event Type
Malfunction
Date Received
January 9, 2013
Date of Event
October 12, 2012
Manufacturer
ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION
Product Code
KRG
PMA / PMN Number
P030054
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

ALL INFORMATION PROVIDED BY MANUFACTURER, NO MEDWATCH FORM WAS RECEIVED. (B)(4).

Description of Event or Problem · 1

IT WAS REPORTED THAT SMOKE WAS NOTED COMING OUT OF THE PROGRAMMER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
12501 MERLIN PROGRAMMER PACEMAKER PROGRAMMER KRG ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION 3650 NA

Patients

Seq Age Sex Outcome Treatment
1