FDA Adverse Event Malfunction Summary report: N

SPRINT QUATTRO SECURE

MDR report key: 2201688 · Received August 11, 2011

Report

Report Number
2649622-2011-11168
Event Type
Malfunction
Date Received
August 11, 2011
Date of Event
May 9, 2011
Manufacturer
MEDTRONIC PUERTO RICO, INC.
Product Code
LWS
PMA / PMN Number
P920015/S24
Removal / Correction Number
ASKU
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
KY, 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. EVALUATION SUMMARY: (B)(4): THE ACTUAL DEVICE AND LEAD WERE NOT RECEIVED FOR EVALUATION. WE DID RECEIVE PERFORMANCE DATA COLLECTED FROM THE DEVICE AND HAVE ANALYZED THE DATA. A 2 - PORS (POWER ON RESET) ON (B)(4)-2011. A 1- PATIENT ALERT FOR DEVICE CIRCUIT ERROR ON (B)(4)-2011 10:02:20. DAILY PACE IMPEDANCE TREND DATA SHOW THE IMPEDANCE FOR VENTRICULAR PACE BI IMPEDANCE= 4047 OHMS AND ATRIAL PACE BI IMPEDANCE=4047 OHMS BETWEEN (B)(4)-2011.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT HAD SURGERY FOR BREAST CANCER AND THERE WAS AN ELECTRICAL RESET. THE RIGHT ATRIAL (RA) LEAD THE RIGHT VENTRICULAR (RV) LEAD AND BOTH LEFT VENTRICULAR (LV) LEADS SHOWED HIGH RESISTANCE/IMPEDANCE. IT WAS ALSO REPORTED THAT THE POWER-ON-RESET WAS CAUSED BY A POWER SUPPLY ISSUE WHICH MAY BE RELATED THE PATIENT'S SURGERY. THE FOLLOW-UP INFORMATION OBTAINED COULD NOT CONFIRM IF THERE WAS ANY INTERVENTION DONE. THE SYSTEM 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 ASKU

Patients

Seq Age Sex Outcome Treatment
1 63 YR Other