LEAD MODEL 302
Report
- Report Number
- 1644487-2023-00721
- Event Type
- Malfunction
- Date Received
- June 6, 2023
- Date of Event
- December 1, 2022
- Report Date
- June 6, 2023
- Manufacturer
- CYBERONICS - HOUSTON
- Product Code
- LYJ
- PMA / PMN Number
- P970003
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- UK
- Reporter Occupation
- PHYSICIAN
- Health Professional
- Yes
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 DURING A VISIT, HIGH IMPEDANCE WAS OBSERVED. IT WAS DISCUSSED IN THE REPORT THAT THE PATIENT WOULD NEED TO BE REFERRED FOR A REVISION. THE PATIENT HAD NO COMPLAINTS OF PAIN OR CHANGE IN SEIZURE PATTERN. PER THE REPORT, THE PATIENT WAS SEEN IN FEBRUARY AND THE VNS WAS OK. X-RAYS WERE DONE, AND THE LEAD WAS SEEN INTACT. SESSION REPORTS WERE ALSO INCLUDED WITH THE REPORT. NO KNOWN RELEVANT SURGICAL INTERVENTION HAS OCCURRED TO DATE. NO OTHER RELEVANT INFORMATION HAS BEEN RECEIVED TO DATE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 570579 | LEAD MODEL 302 | LEAD | LYJ | CYBERONICS - HOUSTON | 302-20 | 2447 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 21 YR | Male |