NAVLOCK
Report
- Report Number
- 1723170-2025-03470
- Event Type
- Malfunction
- Date Received
- October 15, 2025
- Date of Event
- July 22, 2025
- Report Date
- October 15, 2025
- Manufacturer
- MEDTRONIC NAVIGATION, INC.
- Product Code
- KCT
- UDI-DI
- 00653159011696
- PMA / PMN Number
- K960738
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- JA
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
- Health Professional
- Yes
Narratives
H3, H6: THE CONTAINER, LOT NUMBER: 2031696, WAS RETURNED TO THE MANUFACTURER FOR ANALYSIS. REPORTED PROBLEM WAS CONFIRMED. THE BRACKETS INSIDE THE CONTAINER WERE DELAMINATING, AND SOME OF THE BRACKETS WERE BENT. THE REPORTED EVENT COULD BE DUPLICATED BY MEDTRONIC PERSONNEL. CODES B01, C07, AND D02 ARE APPLICABLE TO THIS ANALYSIS. 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.
MEDTRONIC RECEIVED INFORMATION REGARDING A NAVIGATION SYSTEM BEING USED OUTSIDE OF A PROCEDURE. IT WAS REPORTED THAT THERE WAS PEELING OF THE CASE PLATING AND DEFORMATION FOR THE THREE CONTAINERS. THERE WAS NO PATIENT INVOLVEMENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 2289287 | NAVLOCK | STERILIZATION WRAP CONTAINERS, TRAYS, CASSETTE | KCT | MEDTRONIC NAVIGATION, INC. | 9734692 | 2031696 | 00653159011696 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown |