FDA Adverse Event Death Summary report: N

LIFELINE

MDR report key: 1652806 · Received April 5, 2010

Report

Report Number
2124215-2010-06792
Event Type
Death
Date Received
April 5, 2010
Date of Event
March 11, 2010
Report Date
March 11, 2010
Manufacturer
GUIDANT ANGLETON/ST. PAUL
Product Code
DTB
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
WI, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THIS PRODUCT WILL BE RETAINED BY THE MEDICAL EXAMINER AND WILL NOT BE RETURNED. NO ADDITIONAL INFORMATION IS AVAILABLE AT THIS TIME. IF THE PRODUCT IS RETURNED, OR IF ADDITIONAL INFORMATION BECOMES AVAILABLE, THIS EVENT WILL BE UPDATED.

Description of Event or Problem · 1

BOSTON SCIENTIFIC CRM RECEIVED INFORMATION THAT THIS PATIENT HAD PREVIOUSLY BEEN SEEN A DIFFERENT INSTITUTION FOR A PULMONARY EMBOLISM AND UNDERWENT A SEPARATE PROCEDURE PRIOR TO THIS EVENT. UPON DISCHARGE FROM THE PREVIOUS PROCEDURE, THE PATIENT BECAME SEPTIC AND DEVELOPED A SYSTEMIC INFECTION WHICH INVOLVED THE CHRONIC PACING LEADS. THE PATIENT HAD ALSO DEVELOPED VEGETATION IN THE RIGHT ATRIUM (RA). A REVISION PROCEDURE WAS SCHEDULED. DURING THE REVISION PROCEDURE, THE PATIENT WAS PLACED ON THE CARDIOPULMONARY BYPASS MACHINE FOR LASER LEAD EXTRACTION TO REMOVE THE INFECTED PACING SYSTEM AND REMOVE THE VEGETATION FROM THE RA. AFTER THE CHRONIC SYSTEM WAS EXPLANTED, A NEW DEVICE AND TWO EPICARDIAL LEADS WERE IMPLANTED. WHILE ATTEMPTED TO REMOVE THE PATIENT FROM THE CARDIOPULMONARY BYPASS MACHINE, THE PATIENT'S PREVIOUSLY NOTED PULMONARY EMBOLISM BECAME EXACERBATED, AND THE PATIENT EXPIRED AS A RESULT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 LIFELINE IMPLANTABLE LEAD DTB GUIDANT ANGLETON/ST. PAUL 476-01

Patients

Seq Age Sex Outcome Treatment
1 67 YR Death S603| 476-01| 2550| 480-01| (B) (4)| 4047| 284-02| 253-05| 4046