MAUDE Adverse Event Report: ST. JUDE MEDICAL, BRASIL LTDA. (PAMPULHA) EPIC STENTED TISSUE VALVE; HEART-VALVE, NON-ALLOGRAFT TISSUE

Device Problem Obstruction of Flow (2423)

Patient Problems Hemorrhage/Bleeding (1888); Thrombosis (2100)

Event Type  Injury  

Manufacturer Narrative

The results/method and conclusion codes along with investigation results will be provided in the final report.

Event Description

Reference manufacturer report number: 2648612-2020-00127, 2648612-2020-00128.The article "which is the best prosthesis in an isolated or combined tricuspid valve replacement?" was reviewed.This research article is a retrospective multi center experience to compare the long-term results of mechanical and biological prostheses in patients who underwent isolated or combined tricuspid valve replacement.Edwards lifesciences pericardial tissue heart valve; medtronic hancock ii porcine heart valve, mosaic porcine bioprosthesis and mechanical heart valves; abbott epic serial model tissue heart valve and masters series mechanical heart valve were associated to the study.The article concluded that biological prostheses may be an optimal choice for patients, especially for patients without ebstein¿s anomaly, in isolated tricuspid valve replacement.The primary author of the article is peng liu, md of department of cardiovascular surgery, fuwai central china cardiovascular hospital, henan province people¿s hospital, henan cardiovascular hospital and zhengzhou university, zhengzhou, henan, china.The correspondence author is si chen, md of department of cardiovascular surgery, union hospital, huazhong university of science and technology with the corresponding email: steffengloekler@gmail.Com.

Manufacturer Narrative

This report is a duplicate report to 3001883144-2020-00114.The final report will be submitted under 3001883144-2020-00114.

• Brand Name: EPIC STENTED TISSUE VALVE
• Type of Device: HEART-VALVE, NON-ALLOGRAFT TISSUE
• Manufacturer (Section D): ST. JUDE MEDICAL, BRASIL LTDA. (PAMPULHA); rua professor jose vieira de mendonça 1301; engenho nogueira - belo horizonte - mg; belo horizonte 31310 -260; BR 31310-260
• MDR Report Key: 10900604
• MDR Text Key: 218205064
• Report Number: 3001883144-2020-00113
• Device Sequence Number: 1
• Product Code: LWR
• Combination Product (y/n): N
• PMA/PMN Number: P040021
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: foreign,health professional,l
• Type of Report: Initial,Followup
• Report Date: 01/12/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 11/25/2020
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Was Device Available for Evaluation?: No
• Was the Report Sent to FDA?: No
• Date Manufacturer Received: 12/01/2020
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1
• Patient Outcome(s): Required Intervention
• Patient Age: 41 YR