FDA Adverse Event Death Summary report: N

SPRINT FIDELIS

MDR report key: 1850494 · Received October 1, 2010

Report

Report Number
2649622-2010-09080
Event Type
Death
Date Received
October 1, 2010
Date of Event
September 18, 2007
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
MN, US
Reporter Occupation
ATTORNEY

Narratives

Additional Manufacturer Narrative · 1

THIS EVENT INVOLVES A LEGAL CASE IN PROGRESS OR POTENTIAL LITIGATION. THE PROPRIETARY NATURE OF THE EVENT MAY AFFECT FOLLOW UP EFFORTS. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. THE DEVICE IS PART OF THE ADVISORY FOR THIS MODEL. OUR RECORDS INDICATE THE PATIENT EXPIRED MORE THAN ONE YEAR AGO. WE HAVE NO INFORMATION FROM A HEALTH CARE PROFESSIONAL TO SUGGEST THE DEATH WAS DEVICE RELATED. IT IS NOT KNOWN IF THE DEVICE WAS EXPLANTED POST-MORTEM. THE CAUSE OF DEATH HAS BEEN RESEARCHED BUT HAS NOT BEEN RECEIVED.

Description of Event or Problem · 1

ATTORNEY ALLEGES THAT "ON (B)(6) 2007, (PATIENT) WAS IMPLANTED WITH A SPRINT FIDELIS LEAD, MODEL 6949" AND AS A RESULT OF THE LEAD, PATIENT "HAS SUSTAINED AND WILL CONTINUE TO SUSTAIN SEVERE PHYSICAL INJURIES AND/OR DEATH, SEVERE EMOTIONAL DISTRESS AND PHYSICAL MANIFESTATIONS THEREOF, MENTAL ANGUISH, ECONOMIC LOSSES AND OTHER DAMAGES. (PATIENT) DIED AS A DIRECT AND PROXIMATE RESULT OF DEFECTS" IN SPRINT FIDELIS LEAD. THERE IS NO ALLEGATION FROM A HEALTH CARE PROFESSIONAL THAT THE DEATH WAS DEVICE RELATED. THE CAUSE OF DEATH HAS BEEN REQUESTED AND NOT RECEIVED.

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 72 YR Death D154VRC IMPLANTABLE PACEMAKER/CARDIO/DEFIB