FDA Adverse Event Malfunction Summary report: N

MELODY TRANSCATHER PULMONARY VALVE

MDR report key: 6641312 · Received June 14, 2017

Report

Report Number
2025587-2017-00969
Event Type
Malfunction
Date Received
June 14, 2017
Date of Event
February 25, 2016
Report Date
May 31, 2017
Manufacturer
MEDTRONIC HEART VALVES DIVISION
Product Code
NPV
PMA / PMN Number
P140017
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

CITATION: GHOBRIAL J, ABOULHOSN J. IMPACT OF RIGHT-SIDED-CATHETER-BASED VALVE IMPLANTATION ON DECISION-MAKING IN CONGENITAL HEART DISEASE. CURR CARDIOL REP. 2016 APR;18(4):33. DOI: 10.1007/S11886-016-0712-2. EARLIEST DATE OF E-PUBLISH/PUBLISH USED FOR EVENT DATE. NO UNIQUE DEVICE IDENTIFIER (SERIAL/LOT) NUMBERS WERE PROVIDED; WITHOUT THIS INFORMATION IT CANNOT BE DETERMINED WHETHER THIS EVENT HAS BEEN PREVIOUSLY REPORTED. A GOOD FAITH EFFORT WILL BE MADE TO OBTAIN THE APPLICABLE INFORMATION RELEVANT TO THE REPORT. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Additional Manufacturer Narrative · 1

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

Description of Event or Problem · 1

MEDTRONIC RECEIVED INFORMATION VIA LITERATURE META-ANALYSIS REGARDING THE IMPACT OF RIGHT-SIDED CATHETER BASED VALVE IMPLANTATION. ALL DATA WERE COLLECTED FROM MULTIPLE CENTERS. THE STUDY POPULATION INCLUDED AN UNDETERMINED AMOUNT OF PATIENTS IMPLANTED WITH MEDTRONIC MELODY TRANSCATHETER PULMONARY VALVES (SERIAL NUMBERS NOT PROVIDED). AMONG ALL PATIENTS DEVICE MALFUNCTIONS INCLUDED: STENT FRACTURE. BASED ON THE AVAILABLE INFORMATION, AN UNDETERMINED AMOUNT WERE ATTRIBUTED TO MEDTRONIC PRODUCT. NO ADDITIONAL ADVERSE PATIENT EFFECTS WERE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
422110 MELODY TRANSCATHER PULMONARY VALVE PULMONARY VALVE PROSTHESIS PERCUTANEOUSLY DELIVERED NPV MEDTRONIC HEART VALVES DIVISION PB 10

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention