FDA Adverse Event Injury Summary report: N

SOLOGRIP III HANDPIECE

MDR report key: 3700163 · Received March 26, 2014

Report

Report Number
2950727-2014-00003
Event Type
Injury
Date Received
March 26, 2014
Date of Event
November 30, 2013
Report Date
March 21, 2014
Manufacturer
CARDIOGENESIS CORPORATION
Product Code
MNO
PMA / PMN Number
P970029
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THIS INVESTIGATION IS CURRENTLY ONGOING. ANY ADDITIONAL INFORMATION WILL BE PROVIDED IN THE FOLLOW-UP REPORT.

Additional Manufacturer Narrative · 1

THIS COMPLAINT WAS REPORTED THROUGH THE ANGINA RELIEF REGISTRY. THE PATIENT WAS RE-HOSPITALIZED FOR HEART FAILURE NINE DAYS AFTER THE CABG+TMR PROCEDURE. THE PATIENT WAS ANGINA-FREE AT THE 30-DAY FOLLOW-UP. ACCORDING TO DOCUMENTATION, ALL AVAILABLE RECORDS SHE THE HANDPIECE WAS CORRECTLY ASSEMBLED FROM SOUND COMPONENTS AND WERE INSPECTED TO SPECIFICATIONS. HOSPITAL READMISSION RATES DUE TO HEART FAILURE FOR PATIENTS UNDERGOING CABG WITH ADJUNCTIVE TMR HAVE ALSO BEEN REPORTED; AT 30 DAYS HOSPITAL READMISSION DUE TO HEART FAILURE WAS 5% IN TMR + CABG PATIENTS AND 6% FOR PATIENTS WHO UNDERWENT CABG ALONE. HEART FAILURE IS A COMMONLY REPORTED ADVERSE EVENT AFTER CABG PROCEDURES WITH OR WITHOUT ADJUNCTIVE TMR. THIS PATIENT'S PRE-OPERATIVE MEDICAL HISTORY INCLUDED VARIOUS RISK FACTORS THAT MAY INCREASE THE RISK OF HEART FAILURE AFTER CABG.

Description of Event or Problem · 1

THE PATIENT WAS RE-HOSPITALIZED FOR HEART FAILURE NINE DAYS AFTER THE CABG+TMR PROCEDURE.

Description of Event or Problem · 1

THE PATIENT WAS RE-HOSPITALIZED FOR HEART FAILURE NINE DAYS AFTER THE CABG+TMR PROCEDURE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
178090 SOLOGRIP III HANDPIECE TRANSMYOCARDIAL REVASCULARIZATION HANDPIECE MNO CARDIOGENESIS CORPORATION HP-SG3

Patients

Seq Age Sex Outcome Treatment
1 45 YR Other