FDA Adverse Event Malfunction Summary report: N

TENDRIL STS

MDR report key: 2013913 · Received March 10, 2011

Report

Report Number
2017865-2011-01688
Event Type
Malfunction
Date Received
March 10, 2011
Date of Event
December 22, 2010
Manufacturer
ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION
Product Code
DTB
PMA / PMN Number
NA
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

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 ONE DAY POST IMPLANT, THE RIGHT VENTRICULAR LEAD EXHIBITED BIPOLAR IMPEDANCE OF 2600 OHMS AND HIGH CAPTURE THRESHOLD AT 3.5 V. IN UNIPOLAR, IMPEDANCE WAS 430 OHMS AND THRESHOLDS IMPROVED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TENDRIL STS PERMANENT PACEMAKER ELECTRODE DTB ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION 2088TC/52 NA

Patients

Seq Age Sex Outcome Treatment
1 87 YR