FDA Adverse Event Malfunction Summary report: N

ATTAIN ABILITY

MDR report key: 2811707 · Received October 31, 2012

Report

Report Number
2649622-2012-15886
Event Type
Malfunction
Date Received
October 31, 2012
Date of Event
September 10, 2012
Manufacturer
MEDTRONIC PUERTO RICO, INC.
Product Code
OJX
PMA / PMN Number
P080006
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NC, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THE INFORMATION SUBMITTED REFLECTS ALL RELEVANT DATA RECEIVED. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE LEFT VENTRICULAR LEAD HAD HIGH THRESHOLDS AND NO CAPTURE. THE RIGHT VENTRICULAR LEAD ALSO HAD HIGH THRESHOLDS. THE LEADS REMAIN IN USE. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ATTAIN ABILITY IMPLANTABLE PACING LEAD OJX MEDTRONIC PUERTO RICO, INC. 4196

Patients

Seq Age Sex Outcome Treatment
1 60 YR Other C2TR01: IMPLANTABLE PULSE GENERATOR| 4076: IMPLANTABLE PACING LEAD