FDA Adverse Event Injury Summary report: N

DURAN ANCORE RING

MDR report key: 5743449 · Received June 22, 2016

Report

Report Number
2025587-2016-00921
Event Type
Injury
Date Received
June 22, 2016
Date of Event
March 19, 2016
Report Date
May 26, 2016
Manufacturer
MEDTRONIC HEART VALVES DIVISION
Product Code
KRH
PMA / PMN Number
K960356
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

CITATION: ROBERTS W ET AL. MITRAL VALVE REPLACEMENT AFTER FAILED MITRAL RING INSERTION WITH OR WITHOUT LEAFLET/CHORDAL REPAIR FOR PURE MITRAL REGURGITATION. AM J CARDIOL. 2016 JUN 1;117(11):1790-807. DATE OF PUBLISH USED FOR EVENT DATE. NO UNIQUE DEVICE IDENTIFIER (SERIAL/LOT) NUMBERS WERE PROVIDED; WITHOUT THIS INFORMATION IT COULD NOT BE DETERMINED WHETHER THESE OBSERVATIONS HAVE BEEN PREVIOUSLY REPORTED.

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 REGARDING UNFORTUNATE CONSEQUENCES OF MITRAL VALVE REPAIR WITH RING OR BAND IMPLANTATION. THE STUDY POPULATION INCLUDED 29 PATIENTS (PREDOMINANTLY MALE; MEAN AGE 61 YEARS), FOUR OF WHICH WERE IMPLANTED WITH MEDTRONIC DURAN RING AND ONE OF WHICH WAS IMPLANTED WITH MEDTRONIC ATS SIMULUS SEMI-RIGID BAND. THE SERIAL NUMBERS WERE NOT PROVIDED. PATIENT 1: A (B)(6) MALE WITH MITRAL VALVE PROLAPSE WAS IMPLANTED WITH A 33-MM DURAN RING. SIXTEEN DAYS POST-IMPLANT LEAFLET REPAIR BREAKDOWN WAS NOTED. THE RING WAS EXPLANTED, A MECHANICAL VALVE WAS IMPLANTED, AND A CORONARY ARTERY BYPASS GRAFT (CABG) PROCEDURE WAS PERFORMED. NO ADDITIONAL ADVERSE PATIENT EFFECTS WERE REPORTED REGARDING MEDTRONIC PRODUCT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
396603 DURAN ANCORE RING RING, ANNULOPLASTY KRH MEDTRONIC HEART VALVES DIVISION 620R

Patients

Seq Age Sex Outcome Treatment
1 49 YR Life Threatening| R