VITALITY 2
Report
- Report Number
- 2124215-2012-16763
- Event Type
- Death
- Date Received
- December 17, 2012
- Date of Event
- November 20, 2012
- Report Date
- December 18, 2012
- Manufacturer
- GUIDANT CRM CLONMEL IRELAND
- Product Code
- LWS
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA
- Reporter Occupation
- PHYSICIAN
Narratives
BOSTON SCIENTIFIC RECEIVED INFORMATION THAT THE LOCAL REPRESENTATIVE SPOKE DIRECTLY WITH THE PHYSICIAN. ACCORDING TO THE PHYSICIAN, THE EXTRACTION PROCEDURE ASSOCIATED WITH THE TEAR OF THE SUPERIOR VENA CAVA (SVC) DID CONTRIBUTE TO THE PATIENT'S DEATH. THE DOCUMENTED CAUSE OF DEATH WAS RELATED TO REFRACTORY ACIDOSIS. THE REPORTED INFECTION DID NOT CAUSE OR CONTRIBUTE TO THE PATIENT'S DEATH.
AS NO FURTHER INFORMATION CONCERNING THIS REPORT IS EXPECTED, OUR INVESTIGATION IS COMPLETE. THIS INVESTIGATION WILL BE UPDATED SHOULD FURTHER INFORMATION BE PROVIDED.
BOSTON SCIENTIFIC RECEIVED INFORMATION THAT THIS PATIENT WAS PRESENTED TO THE ELECTROPHYSIOLOGY (EP) LABORATORY FOR EXTRACTION OF THIS PATIENT'S IMPLANTABLE CARDIOVERTER DEFIBRILLATOR (ICD) AND TRANSVENOUS LEAD SYSTEM DUE TO INFECTION. THE PATIENT PAST IMPLANT HISTORY IS SIGNIFICANT FOR A RECENT SUBCUTANEOUS IMPLANTABLE CARDIOVERTER DEFIBRILLATOR (S-ICD) IN PREPARATION FOR THE EXTRACTION PROCEDURE. DURING THE EXTRACTION PROCEDURE, THE SUPERIOR VENA CAVA (SVC) WAS TORN. THE SVC WAS REPAIRED AND THE ENTIRE SYSTEM WAS SUCCESSFULLY EXTRACTED. SUBSEQUENTLY, BOSTON SCIENTIFIC RECEIVED INFORMATION THAT THIS PHYSICIAN CONTACTED THE LOCAL REPRESENTATIVE TO REPORT THAT THIS PATIENT HAD DIED FOUR DAYS LATER.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | VITALITY 2 | IMPLANTABLE CARDIOVERTER DEFIBRILLATOR | LWS | GUIDANT CRM CLONMEL IRELAND | T165 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 66 YR | Death | T165| 0185| 4086| 0184 |