FDA Adverse Event Malfunction Summary report: N

NAVLOCK

MDR report key: 23211470 · Received October 3, 2025

Report

Report Number
1723170-2025-03385
Event Type
Malfunction
Date Received
October 3, 2025
Date of Event
July 30, 2025
Report Date
October 3, 2025
Manufacturer
MEDTRONIC NAVIGATION, INC.
Product Code
OLO
PMA / PMN Number
K124004
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

H3, H6) THE 9734680 (LOT: 180719) PROBE WAS RETURNED TO THE MANUFACTURER FOR EVALUATION. IT WAS FOUND THAT THE TIP OF THE PROBE WAS TWISTED. THE PROBE INSERTED, ROTATED, AND RELEASED FROM A KNOWN GOOD NAVLOCK TRACKER WITHOUT ISSUE. CODES B01, C07, AND D02 ARE APPLICABLE. MEDTRONIC SUBMITS THIS REPORT TO COMPLY WITH FDA REGULATIONS 21 CFR PARTS 4 AND 803. MEDTRONIC HAS MADE REASONABLE EFFORTS TO PROVIDE AS MUCH RELEVANT INFORMATION AS IS AVAILABLE TO THE COMPANY AS OF THE SUBMISSION DATE OF THIS REPORT. THIS REPORT DOES NOT CONSTITUTE AN ADMISSION OR A CONCLUSION BY FDA, MEDTRONIC, OR ITS EMPLOYEES THAT THE DEVICE, MEDTRONIC, OR ITS EMPLOYEE CAUSED OR CONTRIBUTED TO THE EVENT DESCRIBED IN THE REPORT. ANY REQUIRED FIELDS THAT ARE UNPOPULATED ARE BLANK BECAUSE THE INFORMATION IS CURRENTLY UNKNOWN OR UNAVAILABLE. MEDTRONIC WILL SUBMIT A SUPPLEMENTAL REPORT IF ADDITIONAL RELEVANT INFORMATION BECOMES KNOWN.

Description of Event or Problem · 0

MEDTRONIC RECEIVED INFORMATION REGARDING A NAVIGATION SYSTEM BEING USED OUTSIDE OF A PROCEDURE. IT WAS REPORTED THAT THE PROBE WAS D EFORMED. THERE WAS NO PATIENT INVOLVEMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1588384 NAVLOCK ORTHOPEDIC STEREOTAXIC INSTRUMENT OLO MEDTRONIC NAVIGATION, INC. 9734680 180719

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown