FDA Adverse Event Injury Summary report: N

VALVE CONTEGRA

MDR report key: 6537074 · Received May 2, 2017

Report

Report Number
2025587-2017-00720
Event Type
Injury
Date Received
May 2, 2017
Date of Event
April 3, 2012
Report Date
April 24, 2017
Manufacturer
MEDTRONIC HEART VALVES DIVISION
Product Code
MWH
PMA / PMN Number
H020003
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
GM
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

CITATION: RÜFFER A ET AL. MID-TERM EXPERIENCE WITH THE HANCOCK PORCINE-VALVED DACRON CONDUIT FOR RIGHT VENTRICULAR OUTFLOW TRACT REC ONSTRUCTION. EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY 42 (2012) 988¿995. DOI:10.1093/EJCTS/EZS103 ADVANCE ACCESS PUBLICATION 3 APRIL 2012 EARLIEST 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 A TEN YEAR EXPERIENCE WITH THE HANCOCK VALVED CONDUIT IN RIGHT VENTRICULAR OUTFLOW TRACT (RVOT) RECONSTRUCTION. ALL DATA WERE COLLECTED FROM A SINGLE CENTER BETWEEN AUGUST 2000 AND JULY 2010. THE STUDY POPULATION INCLUDED 63 PATIENTS (PREDOMINANTLY MALE, MEAN AGE 13 YEARS, MEDIAN WEIGHT 44 KG), ALL OF WHICH WERE IMPLANTED WITH MEDTRONIC HANCOCK VALVED CONDUIT. WITHIN THIS POPULATION SIX PATIENTS HAD MEDTRONIC CONTEGRA CONDUIT AND EIGHT PATIENTS HAD HANCOCK CONDUIT PREVIOUSLY IMPLANTED. NO SERIAL NUMBERS WERE PROVIDED FOR ANY OF THE MEDTRONIC PRODUCT. NO FURTHER DETAILS WERE PROVIDED REGARDING THE INTERVENTION TO REPLACE THE CONTEGRA CONDUIT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
317575 VALVE CONTEGRA CONDUIT,VALVED,PULMONIC MWH MEDTRONIC HEART VALVES DIVISION CONTEGRA

Patients

Seq Age Sex Outcome Treatment
1 13 YR Required Intervention