FDA Adverse Event Injury Summary report: N

SPRINT QUATTRO SECURE

MDR report key: 2203410 · Received August 11, 2011

Report

Report Number
2649622-2011-11867
Event Type
Injury
Date Received
August 11, 2011
Manufacturer
MEDTRONIC PUERTO RICO, INC.
Product Code
LWS
PMA / PMN Number
P920015/S24
Removal / Correction Number
Z-0475-2011
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OK, 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 FULL LEAD WAS RETURNED IN SEGMENTS AND ANALYZED. PRIMARY ANALYSIS REVEALED NO ANOMALIES. HOWEVER, THE DISTAL CONDUCTOR WAS DISTORTED. THE INNER AND OUTER TUBING WAS KINKED/BUCKLED. THE OUTER TUBING OVERLAY WAS MELTED AND THE OUTER INSULATION WAS TORN. THE OUTER INSULATION HAD A COSMETIC CUT AND COSMETIC DEPRESSION. ALL INSULATORS WERE BREACHED CUT. THE LEAD APPEARED STRETCHED. VISUAL ANALYSIS REVEALED THAT THERE WAS APPARENT EXPLANT DAMAGE.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE LEFT VENTRICULAR (LV) LEAD AND RIGHT VENTRICULAR (RV) LEAD HAD HIGH THRESHOLDS. THE LV LEAD WAS CAPPED AND REPLACED. THE RV LEAD WAS EXPLANTED AND REPLACED. IT WAS ALSO REPORTED THAT DURING THE IMPLANT ATTEMPT, THE LV LEAD HAD POSITIONING DIFFICULTIES DUE TO PATIENT ANATOMY. THE LEAD WAS IMPLANTED AND IS STILL 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 Hospitalization| R 5076 IMPLANTABLE PACING LEAD| (B)(4) IMPLANTABLE PACEMAKER/CARDIO/DEFIB