FDA Adverse Event Death Summary report: N

TENDRIL STS

MDR report key: 6141832 · Received December 2, 2016

Report

Report Number
2017865-2016-07520
Event Type
Death
Date Received
December 2, 2016
Date of Event
October 26, 2016
Report Date
November 7, 2016
Manufacturer
ST. JUDE MEDICAL, INC.(CRM-SYLMAR)
Product Code
NVN
PMA / PMN Number
P960013
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4)

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT HAS DECEASED. THERE IS NO KNOWN ALLEGATION FROM A HEALTH CARE PROFESSIONAL THAT SUGGESTS THE DEATH WAS DEVICE RELATED. THE CAUSE OF DEATH WAS UNKNOWN. NO ADDITIONAL INFORMATION WAS AVAILABLE AT THIS TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
791322 TENDRIL STS PERMANENT PACEMAKER ELECTRODE NVN ST. JUDE MEDICAL, INC.(CRM-SYLMAR) 2088TC/52 A000011865

Patients

Seq Age Sex Outcome Treatment
1 87 YR Death (B)(4)| (B)(4)