FDA Adverse Event Injury Summary report: N

CONCERTO CRT-D DR

MDR report key: 2952990 · Received February 9, 2013

Report

Report Number
3004209178-2013-01853
Event Type
Injury
Date Received
February 9, 2013
Report Date
December 13, 2012
Manufacturer
MEDTRONIC MED REL MEDTRONIC PUERTO RICO
Product Code
NIK
PMA / PMN Number
P010031
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MN, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THIS REPORT IS BASED SOLELY ON DEVICE 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. CONCOMITANT PRODUCTS: 5076 IMPLANTABLE PACING LEAD, (B)(6) 2008; 6947 IMPLANTABLE DEFIBRILLATOR LEAD, (B)(6) 2007; 3023 INTERSTIM URINARY MGU IPG, (B)(6) 2006; 3031A NEURO PROGRAMMER, (B)(6) 2006; 3095-10 NEURO EXTENSION, (B)(6) 2006; 3093-28 INTERSTIM URINARY MGU LEAD, (B)(6) 2006. (B)(4). EVALUATION SUMMARY: (B)(4), THE DEVICE WAS RETURNED AND ANALYZED. A HIGH CURRENT DRAIN CONDITION WAS FOUND DURING DEVICE ANALYSIS. ELECTRICAL ANALYSIS REVEALED THE CAUSE OF THE HIGH CURRENT DRAIN WAS CURRENT LEAKAGE IN THE BATTERY FILTER CAPACITORS.

Description of Event or Problem · 1

THE DEVICE WAS RETURNED TO THE MANUFACTURER AFTER BEING EXPLANTED DUE TO NORMAL BATTERY DEPLETION. THE DEVICE SUBSEQUENTLY TESTED OUT OF SPECIFICATION DURING MANUFACTURER'S ANALYSIS. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
56066 CONCERTO CRT-D DR DEFIBRILLATOR, AUTOMATIC IMPLANTABLE CARDIOVERTER, WITH CARDIAC RESYNCHRONIZATIO NIK MEDTRONIC MED REL MEDTRONIC PUERTO RICO C154DWK

Patients

Seq Age Sex Outcome Treatment
1 00067 YR Hospitalization| R 4193 IMPLANTABLE PACING LEAD