FDA Adverse Event Injury Summary report: N

PULSE GEN MODEL 1000

MDR report key: 16283452 · Received February 2, 2023

Report

Report Number
1644487-2023-00111
Event Type
Injury
Date Received
February 2, 2023
Date of Event
January 6, 2023
Report Date
February 2, 2023
Manufacturer
CYBERONICS - HOUSTON
Product Code
LYJ
UDI-DI
05425025750405
PMA / PMN Number
P970003
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
PHYSICIAN
Health Professional
Yes

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 PATIENT WAS HOSPITALIZED DUE TO INCREASED SEIZURES. WHILE IN THE HOSPITAL THE DEVICE WAS FOUND TO BE AT NEOS=YES (0-8%) SO THE PATIENT WAS REFERRED FOR A BATTERY REPLACEMENT. PATIENT UNDERWENT GENERATOR REPLACEMENT SURGERY. THE EXPLANTED GENERATOR HAS NOT BEEN RECEIVED BY PRODUCT ANALYSIS TO DATE NO OTHER RELEVANT INFORMATION HAS BEEN RECEIVED TO DATE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
901674 PULSE GEN MODEL 1000 GENERATOR LYJ CYBERONICS - HOUSTON 1000 204960 05425025750405

Patients

Seq Age Sex Outcome Treatment
1 56 YR Female Hospitalization| R