FDA Adverse Event Injury Summary report: N

SJM MECHANICAL HEART VALVE

MDR report key: 1940702 · Received December 22, 2010

Report

Report Number
2648612-2010-00079
Event Type
Injury
Date Received
December 22, 2010
Date of Event
November 27, 2010
Report Date
December 22, 2010
Manufacturer
ST. JUDE MEDICAL PUERTO RICO, INC. (CS)
Product Code
LWQ
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IN
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

IT WAS REPORTED, A PT UNDERWENT A DOUBLE VALVE REPLACEMENT SURGERY. POSTOPERATIVELY, THE PT PRESENTED WITH EXTREME SHORTNESS OF BREATH. AN ECHO SHOWED THE MITRAL VALVE HAD ONE LEAFLET STUCK IN THE CLOSED POSITION AND THE MITRAL VALVE WAS EXPLANTED AND REPLACED WITH A SMALLER ROTATABLE VALVE. THE PATIENT'S CONDITION IS REPORTED TO BE IMPROVING. ADD'L INFO HAS BEEN REQUESTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SJM MECHANICAL HEART VALVE STANDARD HEART VALVE LWQ ST. JUDE MEDICAL PUERTO RICO, INC. (CS) 27M-101

Patients

Seq Age Sex Outcome Treatment
1 16 YR Hospitalization| R