FDA Adverse Event Malfunction Summary report: N

SPRINT QUATTRO SECURE S

MDR report key: 1925988 · Received December 14, 2010

Report

Report Number
2649622-2010-14120
Event Type
Malfunction
Date Received
December 14, 2010
Date of Event
October 21, 2010
Manufacturer
MEDTRONIC PUERTO RICO, INC.
Product Code
LWS
PMA / PMN Number
P920015/S039
Removal / Correction Number
ASKU
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NC, 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. ANALYSIS OF THE DEVICE IS IN PROCESS; THE RESULTS WILL BE FORWARDED WHEN AVAILABLE.

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 AND ANALYZED. ANALYSIS RESULTS REVEALED THAT THE HELIX WAS DISENGAGED FROM THE HELICAL CHANNEL. BLOOD WAS PRESENT IN/ON THE HELIX MECHANISM. THE LEAD IS PART OF THE ADVISORY FOR THIS MODEL.

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING AN IMPLANT, THERE WAS AN ATTEMPT TO ADVANCE THE RIGHT VENTRICULAR LEAD THROUGH A SMALL INTRODUCER (7FR INSTEAD OF 9FR) AND THE TIP WAS POSSIBLY DAMAGED. ANOTHER LEAD WAS IMPLANTED. 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 S IMPLANTABLE TACHY LEAD LWS MEDTRONIC PUERTO RICO, INC. 6935 ASKU

Patients

Seq Age Sex Outcome Treatment
1 77 YR Other 6931 IMPLANTABLE TACHY LEAD| 6931 IMPLANTABLE TACHY LEAD| (B)(4) IMPLANTABLE PACEMAKER/CARDIO/DEFIB| 5076 IMPLANTABLE PACING LEAD| 5076 IMPLANTABLE PACING LEAD