FDA Adverse Event Death Summary report: N

SPRINT FIDELIS

MDR report key: 1669403 · Received April 29, 2010

Report

Report Number
2649622-2010-01891
Event Type
Death
Date Received
April 29, 2010
Date of Event
April 19, 2010
Manufacturer
MEDTRONIC PUERTO RICO, INC.
Product Code
LWS
PMA / PMN Number
P920015/S029
Removal / Correction Number
Z-0067-0070-2008
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IN, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THE INFORMATION SUBMITTED REFLECTS ALL RELEVANT DATA RECEIVED. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. ANALYSIS OF THE DEVICE IS IN PROCESS; THE RESULTS WILL BE FORWARDED WHEN AVAILABLE.

Additional Manufacturer Narrative · 1

THE INFORMATION SUBMITTED REFLECTS ALL RELEVANT DATA RECEIVED. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. EVALUATION SUMMARY (B) (4) ANALYSIS OF THE DEVICE FOUND A HIGH CURRENT DRAIN CONDITION. ELECTRICAL ANALYSIS REVEALED THE CAUSE OF THE HIGH CURRENT DRAIN WAS CURRENT LEAKAGE IN THE BATTERY FILTER CAPACITORS. (B) (4) NO ANOMALIES FOUND. PROXIMAL SEGMENT RETURNED AND ANALYZED.

Description of Event or Problem · 1

IT WAS REPORTED THE PATIENT DIED DURING DEVICE CHANGEOUT AND PROPHYLACTIC LEAD REVISION. DURING THE LASER LEAD EXTRACTION, THE PATIENT "CODED AND DIED." FOLLOW UP WITH MANUFACTURER'S REPRESENTATIVE REPORTED THE CAUSE OF DEATH IS UNKNOWN. THE PATIENT DID BECOME HEMODYNAMICALLY UNSTABLE DURING THE DEVICE CHANGEOUT AND DID NOT MAKE IT TO SURGERY. THERE ARE NO DEVICE ALLEGATIONS AS RELATES TO THE PATIENT DEATH.

Description of Event or Problem · 1

(B) (4)

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SPRINT FIDELIS IMPLANTABLE TACHY LEAD LWS MEDTRONIC PUERTO RICO, INC. 6949 ASKU

Patients

Seq Age Sex Outcome Treatment
1 60 YR Death 4194 IMPLANTABLE PACING LEAD| 5076 IMPLANTABLE PACING LEAD