PULSE GEN MODEL 1000
Report
- Report Number
- 1644487-2022-01483
- Event Type
- Injury
- Date Received
- November 21, 2022
- Date of Event
- October 27, 2022
- Report Date
- November 21, 2022
- Manufacturer
- CYBERONICS - HOUSTON
- Product Code
- LYJ
- UDI-DI
- 05425025750405
- PMA / PMN Number
- P970003
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FL, 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 PATIENT WAS RECENTLY ADMITTED INTO THE HOSPITAL FOR UNKNOWN REASONS. THE PATIENT WAS LAST SEEN BY THEIR NEUROLOGIST ON (B)(6) AND HAD THEIR SETTINGS ADJUSTED BUT THERE WERE NO ISSUES, SO THE NEURO OFFICE IS ALSO UNAWARE OF WHAT ISSUES THE PATIENT IS CURRENTLY EXPERIENCING. NO OTHER RELEVANT INFORMATION HAS BEEN RECEIVED TO DATE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1602517 | PULSE GEN MODEL 1000 | GENERATOR | LYJ | CYBERONICS - HOUSTON | 1000 | 205289 | 05425025750405 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 9 YR | Female | Hospitalization |