FDA Adverse Event Injury Summary report: N

SPRINT QUATTRO SECURE

MDR report key: 2051706 · Received April 12, 2011

Report

Report Number
2649622-2011-05641
Event Type
Injury
Date Received
April 12, 2011
Manufacturer
MEDTRONIC PUERTO RICO, INC.
Product Code
LWS
PMA / PMN Number
P920015/S24
Removal / Correction Number
ASKU
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MN, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

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 LEAD WAS NOT RECEIVED FOR EVALUATION. WE DID RECEIVE PERFORMANCE DATA COLLECTED FROM THE DEVICE AND HAVE ANALYZED THE DATA. OUT OF TOLERANCE SUBTHRESHOLD LEAD IMPEDANCE PATIENT ALERT IS OBSERVED ON (B)(6) 2011. THE IMPEDANCE BEHAVIOR CAN ALSO BE OBSERVED ON THE V PACE BI IMPEDANCE DAILY TREND, WHERE THE IMPEDANCE VALUE INCREASES FROM 589 OHMS ON (B)(6) 2011 TO 4047 OHMS ON THE (B)(6) 2011, WHERE IT REMAINS FOR THE REST OF THE RECORD.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT ALERT WAS TRIGGERED, AND THE PATIENT WAS ADMITTED TO THE EMERGENCY ROOM. THE PATIENT ALSO FELL GETTING OUT OF THE CAR. AN INTERROGATION SHOWED OVERSENSING, HIGH IMPEDANCE, AND HIGH THRESHOLDS. IT WAS ALSO REPORTED THAT THE LEAD INTEGRITY ALERT WAS TRIGGERED. UPON REVISION IT WAS FOUND THE SET SCREW WAS LOOSE. AFTER REPAIR, THE LEAD WAS TESTED AND FOUND TO BE WITHIN NORMAL TOLERANCES. THE DEVICE AND LEAD 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 SPRINT QUATTRO SECURE IMPLANTABLE TACHY LEAD LWS MEDTRONIC PUERTO RICO, INC. 6947 ASKU

Patients

Seq Age Sex Outcome Treatment
1 82 YR Hospitalization| R 1388T COMPETITOR IMPLANTABLE PACING LEAD| 4193 IMPLANTABLE PACING LEAD