FDA Adverse Event Death Summary report: N

CAPSUREFIX NOVUS

MDR report key: 3161957 · Received June 11, 2013

Report

Report Number
2649622-2013-08059
Event Type
Death
Date Received
June 11, 2013
Date of Event
January 19, 2013
Report Date
June 20, 2013
Manufacturer
MPRI
Product Code
DTB
PMA / PMN Number
P930039
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MN, US
Reporter Occupation
OTHER

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. THE DEVICES ASSOCIATED WITH THIS ADVERSE OUTCOME WERE RETURNED FROM AN UNKNOWN SOURCE WITH NO INFORMATION. CONSEQUENTLY, CONTACT INFORMATION TO COMPLETE FOLLOW-UP IS NOT REASONABLY KNOWN. THEREFORE, ATTEMPTS FOR ADDITIONAL INFORMATION CANNOT BE MADE. (B)(4). CONCOMITANT PRODUCTS: C4TR01 IMPLANTABLE PULSE GENERATOR (IPG), IMPLANTED: (B)(6) 2012; 419688 IMPLANTABLE PACING LEAD, IMPLANTED: (B)(6) 2012; 5076-45 IMPLANTABLE PACING LEAD, IMPLANTED: (B)(6) 2011.

Additional Manufacturer Narrative · 1

IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Additional Manufacturer Narrative · 1

PRODUCT EVENT SUMMARY: (B)(4) - THE PROXIMAL SEGMENT OF THE LEAD WAS RETURNED, ANALYZED AND NO ANOMALIES WERE FOUND.

Description of Event or Problem · 1

A BIVENTRICULAR IMPLANTABLE PULSE GENERATOR (IPG) SYSTEM WAS RETURNED TO THE MANUFACTURER FROM AN UNKNOWN SOURCE WITH NO INFORMATION. FURTHER REVIEW OF THE MANUFACTURER¿S DATABASE INDICATED THE PATIENT IS DECEASED AND DIED APPROXIMATELY ELEVEN MONTHS AFTER IMPLANT OF IPG AND LEFT VENTRICULAR LEAD.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
263228 CAPSUREFIX NOVUS ELECTRODE, PACEMAKER, PERMANENT DTB MPRI 5076-52

Patients

Seq Age Sex Outcome Treatment
1 00084 YR Death