FDA Adverse Event Injury Summary report: N

SPRINT

MDR report key: 2813332 · Received October 31, 2012

Report

Report Number
2649622-2012-17243
Event Type
Injury
Date Received
October 31, 2012
Manufacturer
MEDTRONIC PUERTO RICO, INC.
Product Code
LWS
PMA / PMN Number
P920015/S13
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, 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, THE PATIENT RECEIVED MULTIPLE INAPPROPRIATE SHOCKS FROM THE RIGHT VENTRICULAR (RV) LEAD. THE LEAD INTEGRITY ALERT TRIGGERED FOR THE RV LEAD HAVING OVERSENSING OF NOISE DUE TO A SUSPECTED LEAD FRACTURE. THE RV LEAD ALSO HAD HIGH IMPEDANCE. THE RV LEAD WAS EXPLANTED AND REPLACED. NO FURTHER PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SPRINT IMPLANTABLE TACHY LEAD LWS MEDTRONIC PUERTO RICO, INC. 6943

Patients

Seq Age Sex Outcome Treatment
1 71 YR Hospitalization| L| R 5076 IMPLANTABLE PACING LEAD| (B)(4) IMPLANTABLE PACEMAKER/CARDIO/DEFIB