FDA Adverse Event Malfunction Summary report: N

LEAD MODEL 302

MDR report key: 17072286 · Received June 6, 2023

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

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 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