FDA Adverse Event Death Summary report: N

ATTAIN LV

MDR report key: 3220849 · Received July 11, 2013

Report

Report Number
2649622-2013-08194
Event Type
Death
Date Received
July 11, 2013
Date of Event
September 2, 2009
Report Date
July 18, 2013
Manufacturer
MPRI
Product Code
LWP
PMA / PMN Number
P010015
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MN, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

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

Additional Manufacturer Narrative · 1

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

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. CONCOMITANT PRODUCTS: 8042B IMPLANTABLE PULSE GENERATOR (IPG), IMPLANTED: (B)(6) 2009. A 5092-58 IMPLANTABLE PACING LEAD, IMPLANTED: (B)(6) 2001. A 5068 IMPLANTABLE PACING LEAD, IMPLANTED: (B)(6) 2001. (B)(4).

Description of Event or Problem · 1

AN IMPLANTABLE BI-VENTRICULAR 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 SEVEN MONTHS AFTER IPG REPLACEMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
319868 ATTAIN LV PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE LWP MPRI 2187-85

Patients

Seq Age Sex Outcome Treatment
1 00087 YR Death