FDA Adverse Event Death Summary report: N

CAPSURE SP

MDR report key: 1830018 · Received September 10, 2010

Report

Report Number
2649622-2010-08984
Event Type
Death
Date Received
September 10, 2010
Date of Event
July 6, 2010
Manufacturer
MEDTRONIC PUERTO RICO, INC.
Product Code
DTB
PMA / PMN Number
P830061/S12
Removal / Correction Number
ASKU
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THIS REPORT IS BASED SOLELY ON DEVICE RETURN AND ANALYSIS. NO INFORMATION TO SUGGEST A DEVICE-RELATED ADVERSE EVENT OR PRODUCT PROBLEM WAS RECEIVED. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. EVALUATION SUMMARY (B)(4) OUTER INSULATION SEPARATION, ALL CONDUCTORS STRETCHED. PROXIMAL SEGMENT RETURNED AND ANALYZED.

Description of Event or Problem · 1

THE LEAD WAS RETURNED TO THE MANUFACTURER FOLLOWING THE PATIENT'S DEATH, ANALYZED, AND SUBSEQUENTLY TESTED OUT OF SPECIFICATION. THERE IS NO ALLEGATION FROM A HEALTH CARE PROFESSIONAL THAT THE DEATH WAS DEVICE RELATED. THE CAUSE OF DEATH HAS BEEN REQUESTED AND NOT RECEIVED.

Description of Event or Problem · 1

THE LEAD WAS RETURNED TO THE MANUFACTURER FOLLOWING THE PATIENT'S DEATH, ANALYZED, AND SUBSEQUENTLY TESTED OUT OF SPECIFICATION. THERE IS NO ALLEGATION FROM A HEALTH CARE PROFESSIONAL THAT THE DEATH WAS DEVICE RELATED. THE CAUSE OF DEATH HAS BEEN REQUESTED AND NOT RECEIVED. FOLLOW UP WITH THE CLINIC REPORTED THEY LAST SAW THE PATIENT ON (B)(6) 2006 AND THE PATIENT HAD LAST BEEN SEEN IN THE "(B)(6) SYSTEM IN (B)(6) 2006."

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CAPSURE SP IMPLANTABLE PACING LEAD DTB MEDTRONIC PUERTO RICO, INC. 4024 ASKU

Patients

Seq Age Sex Outcome Treatment
1 91 YR Death E2DR21 IMPLANTABLE PULSE GENERATOR| 4568 IMPLANTABLE PACING LEAD