FDA Adverse Event Death Summary report: N

SPRINT QUATTRO SECURE

MDR report key: 1912173 · Received December 2, 2010

Report

Report Number
2649622-2010-12184
Event Type
Death
Date Received
December 2, 2010
Date of Event
October 19, 2009
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
IA, 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) NO ANOMALIES FOUND. (B)(4) PROXIMAL SEGMENT OF THE LEAD RETURNED AND ANALYZED. NO ANOMALIES FOUND. ALL CONDUCTORS STRETCHED, OUTER INSULATION BREACHED CUT AND COSMETIC DEPRESSION, AND VISUAL ANALYSIS PERFORMED ONLY. (B)(4) PROXIMAL SEGMENT OF THE LEAD RETURNED AND ANALYZED. NO ANOMALIES FOUND. PROXIMAL CONDUCTOR STRETCHED, OUTER INSULATION COSMETIC DEPRESSION, APPARENT EXPLANT DAMAGE, AND VISUAL ANALYSIS PERFORMED ONLY. (B)(4) PROXIMAL SEGMENT OF THE LEAD RETURNED AND ANALYZED. NO ANOMALIES FOUND. ALL CONDUCTORS STRETCHED, OUTER INSULATION COSMETIC DEPRESSION, APPARENT EXPLANT DAMAGE, AND VISUAL ANALYSIS PERFORMED ONLY.

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) NO ANOMALIES WERE FOUND. (B)(4) PROXIMAL SEGMENT OF THE LEAD WAS RETURNED AND ANALYZED. NO ANOMALIES WERE FOUND. ALL CONDUCTORS STRETCHED, OUTER INSULATION BREACHED CUT AND COSMETIC DEPRESSION, AND VISUAL ANALYSIS WAS PERFORMED. (B)(4) PROXIMAL SEGMENT OF THE LEAD WAS RETURNED AND ANALYZED. NO ANOMALIES WERE FOUND. PROXIMAL CONDUCTOR STRETCHED, OUTER INSULATION COSMETIC DEPRESSION, APPARENT EXPLANT DAMAGE, AND VISUAL ANALYSIS WAS PERFORMED. (B)(4) PROXIMAL SEGMENT OF THE LEAD WAS RETURNED AND ANALYZED. NO ANOMALIES WERE FOUND. ALL CONDUCTORS STRETCHED, OUTER INSULATION COSMETIC DEPRESSION, APPARENT EXPLANT DAMAGE, AND VISUAL ANALYSIS WAS PERFORMED.

Description of Event or Problem · 1

IT WAS REPORTED THE PATIENT DIED APPROXIMATELY FOUR MONTHS AFTER DEVICE AND LEAD REPLACEMENT. THE CAUSE OF DEATH HAS BEEN REQUESTED AND NOT RECEIVED. BASED ON FOLLOW-UP RECEIVED, THE PATIENT DECLINED AGGRESSIVE TREATMENT IN THE HOSPITAL AND WAS ADMITTED INTO HOSPICE CARE WITH A DIAGNOSIS OF CONGESTIVE HEART FAILURE. THE PATIENT WAS DYSPNEIC AND DISTRESSED. IMPLANTABLE CARDIOVERTOR DEFIBRILLATOR THERAPIES WERE TURNED OFF TEN DAYS PRIOR TO THE PATIENT'S DEATH. PACEMAKER THERAPIES REMAINED ON. THERE IS NO ALLEGATION FROM A HEALTH CARE PROFESSIONAL THAT THE PATIENT'S DEATH WAS DEVICE AND/OR LEAD RELATED.

Description of Event or Problem · 1

IT WAS REPORTED THE PATIENT DIED ON (B)(6) 2009 APPROXIMATELY FOUR MONTHS AFTER DEVICE AND LEAD REPLACEMENT. THE CAUSE OF DEATH HAS BEEN REQUESTED AND NOT RECEIVED.

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 Death