SOLOGRIP III HANDPIECE
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
THIS INVESTIGATION IS CURRENTLY ONGOING. ANY ADDITIONAL INFORMATION WILL BE PROVIDED IN THE FOLLOW-UP REPORT.
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.
THE PATIENT WAS RE-HOSPITALIZED FOR HEART FAILURE NINE DAYS AFTER THE CABG+TMR PROCEDURE.
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 |