FDA Adverse Event Death Summary report: N

PULSE GEN MODEL 1000

MDR report key: 18290648 · Received December 8, 2023

Report

Report Number
1644487-2023-01767
Event Type
Death
Date Received
December 8, 2023
Date of Event
November 14, 2023
Report Date
December 8, 2023
Manufacturer
CYBERONICS - HOUSTON
Product Code
LYJ
UDI-DI
05425025750405
PMA / PMN Number
P970003
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 0

LIVANOVA USA, INC. SUBMITS THIS REPORT TO COMPLY WITH 21 C.F.R. PART 803, THE MEDICAL DEVICE REPORTING REGULATION, BASED ON INFORMATION THAT LIVANOVA HAS OBTAINED, BUT MAY NOT HAVE BEEN ABLE TO INVESTIGATE OR VERIFY PRIOR TO THE DATE THE REPORT WAS REQUIRED BY THE FDA. THIS REPORT DOES NOT CONSTITUTE AN ADMISSION, OR A CONCLUSION BY FDA OR ANYONE ELSE, THAT THE DEVICE, LIVANOVA, OR LIVANOVA'S EMPLOYEES CAUSED OR CONTRIBUTED TO THE EVENT DESCRIBED IN THE REPORT. IN PARTICULAR, THIS REPORT DOES NOT CONSTITUTE AN ADMISSION BY ANYONE THAT THE PRODUCT DESCRIBED IN THIS REPORT HAS ANY "DEFECTS¿ OR "MALFUNCTIONS¿. THESE WORDS ARE INCORPORATED INTO THE FDA 3500A MEDWATCH FORM BY THE FDA, AND LIVANOVA OBJECTS TO THEIR USE.

Description of Event or Problem · 0

IT WAS REPORTED THAT THE MEDICAL EXAMINER PERFORMED AN AUTOPSY ON AN UNKNOWN PATIENT AND DISCOVERED A VNS DEVICE DURING SAID PROCEDURE. IDENTIFICATION OF THE PATIENT WAS MADE POSSIBLE VIA VNS DEVICE INFORMATION. THE MEDICAL EXAMINER NOTED THAT THE CAUSE OF THE DEATH IS CURRENTLY UNKNOWN, BUT POSSIBLY DRUG RELATED. NO OTHER RELEVANT INFORMATION HAS BEEN RECEIVED TO DATE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
222357 PULSE GEN MODEL 1000 GENERATOR LYJ CYBERONICS - HOUSTON 1000 205517 05425025750405

Patients

Seq Age Sex Outcome Treatment
1 21 YR Male Death