PULSE GEN MODEL 1000
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
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.
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 |