FDA Adverse Event Malfunction Summary report: N

TENDRIL ST

MDR report key: 3923376 · Received July 9, 2014

Report

Report Number
2017865-2014-14659
Event Type
Malfunction
Date Received
July 9, 2014
Date of Event
May 6, 2014
Manufacturer
ST. JUDE MEDICAL, INC., CRMD
Product Code
NVN
PMA / PMN Number
NA
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

ALL INFORMATION PROVIDED BY MANUFACTURER, NO MEDWATCH FORM WAS RECEIVED.

Description of Event or Problem · 1

IT WAS REPORTED THAT LOW LEVELS OF NOISE WERE OBSERVED ON THE ASYMPTOMATIC PATIENTS ATRIAL LEAD. THE NOISE COULD BE REPRODUCED THROUGH ISOMETRIC EXERCISES. THE PATIENT DID NOT HAVE AN ACTIVE CARDIOLOGIST AT THE TIME. THE CLINICIAN WOULD PLAN A COURSE OF ACTION ONCE A PHYSICIAN WAS CHOSEN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
401829 TENDRIL ST PERMANENT PACEMAKER ELECTRODE NVN ST. JUDE MEDICAL, INC., CRMD 1882TC/46 NA

Patients

Seq Age Sex Outcome Treatment
1 80 YR