BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CD HORIZON® SPINAL SYSTEM

    MDR report key: 24289574 · Received February 9, 2026

    Report

    Report Number
    3003120897-2026-00218
    Event Type
    Malfunction
    Date Received
    February 9, 2026
    Date of Event
    January 14, 2026
    Report Date
    May 21, 2026
    Manufacturer
    MEDTRONIC SOFAMOR DANEK USA, INC.
    Product Code
    KWP
    PMA / PMN Number
    K132639
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KS
    Reporter Occupation
    PHYSICIAN
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    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. MEDTRONIC WILL SUBMIT A SUPPLEMENTAL REPORT IF ADDITIONAL RELEVANT INFORMATION BECOMES KNOWN.

    Additional Manufacturer Narrative · 0

    H3: PRODUCT ANALYSIS OF PART # 9010000849, LOT # K23F1213 VISUAL AND FUNCTIONAL INSPECTION REVEALED THE INNER SHAFT DOES NOT MOVE WHEN THE LOCKING LEVER IS MOVED. THE C CLIP THAT CONNECTS THE ADJUSTING MECHANISM TO THE INNER SHAFT APPEARS TO HAVE BEEN OVERLOADED AND BROKEN. IT IS POSSIBLE TO OVERLOAD THE CLIP WHEN MAKING TENSION ADJUSTMENTS WHILE THE ROD IS IN PLACE. IT APPEARS THE C CLIP BROKE FROM OVERLOAD. 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

    IT WAS REPORTED THAT THE NEEDLE NEVER DEPLOYED THE CANNULA INTO THE SKIN. THE PINK SLIDE DID NOT MOVE FORWARD AND THE CANNULA WAS NOT VISIBLE WHEN THE POD WAS REMOVED AND NOTICED THAT THE ADHESIVE WAS NOT STICKING WELL. NO IMPACT TO THE PATIENT'S GLUCOSE LEVEL WAS REPORTED. THE POD WAS NOT WORN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    151127 CD HORIZON® SPINAL SYSTEM APPLIANCE, FIXATION, SPINAL INTERLAMINAL KWP MEDTRONIC SOFAMOR DANEK USA, INC. 9010000849 K23F1213

    Patients

    Seq Age Sex Outcome Treatment
    1