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