FDA Adverse Event Malfunction Summary report: N

SPRINT QUATTRO SECURE

MDR report key: 1925603 · Received December 14, 2010

Report

Report Number
2649622-2010-13959
Event Type
Malfunction
Date Received
December 14, 2010
Date of Event
October 2, 2010
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
UT, 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 NO ANOMALIES WERE FOUND. BLOOD/BODY FLUID WAS PRESENT ON SEVERAL CONDUCTORS AND IN/ON THE HELIX MECHANISM AND ITS SLEEVE HEAD. SEVERAL CONDUCTORS AND THE INNER TUBING WERE CUT. THE OUTER INSULATION AND THE OUTER TUBING OVERLAY WERE BREACHED CUT. THE INNER TUBING WAS KINKED/BUCKLED. THE HELIX WAS DISENGAGED FROM THE HELICAL CHANNEL. THE TIP SEAL WAS OBSERVED TO BE OUT OF POSITION. THE LEAD WAS DAMAGED AT IMPLANT.

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING THE IMPLANT ATTEMPT WHILE TRYING TO SEPARATE THE LEAD FROM THE SHEATH THE PHYSICIAN CUT THE LEAD. THE LEAD WAS REMOVED, AND 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 IMPLANTABLE TACHY LEAD LWS MEDTRONIC PUERTO RICO, INC. 6947 ASKU

Patients

Seq Age Sex Outcome Treatment
1 37 YR Other