FDA Adverse Event Injury Summary report: N

SPRINT QUATTRO SECURE

MDR report key: 2790929 · Received October 15, 2012

Report

Report Number
2649622-2012-14474
Event Type
Injury
Date Received
October 15, 2012
Date of Event
August 9, 2012
Manufacturer
MEDTRONIC PUERTO RICO, INC.
Product Code
LWS
PMA / PMN Number
P920015/S24
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 THAT THE RIGHT VENTRICULAR LEAD HAD HIGH IMPEDANCE AND THRESHOLD, OVERSENSING, AND THAT THE LEAD INTEGRITY ALERT HAD TRIPPED. THE PATIENT WAS TAKEN BACK TO SURGERY AND IT WAS NOTED ON FLUORO THAT THE PIN IN THE RV LEAD WAS NOT EXTENDED PAST THE SETSCREW. THE PHYSICIAN REINSERTED THE RV LEAD PIN AND FOUND THE PIN TO BE SECURE. THE LEAD REMAINS 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 SPRINT QUATTRO SECURE IMPLANTABLE TACHY LEAD LWS MEDTRONIC PUERTO RICO, INC. 6947

Patients

Seq Age Sex Outcome Treatment
1 77 YR Hospitalization| R 5076 IMPLANTABLE PACING LEAD| (B)(4) IMPLANTABLE PACEMAKER/CARDIO/DEFIB| 4193 IMPLANTABLE PACING LEAD