BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    M.U.S.T. PEDICLE SCREW SYSTEM

    MDR report key: 23543692 · Received November 13, 2025

    Report

    Report Number
    3005180920-2025-01083
    Event Type
    Malfunction
    Date Received
    November 13, 2025
    Date of Event
    October 15, 2025
    Report Date
    November 13, 2025
    Manufacturer
    MEDACTA INTERNATIONAL SA
    Product Code
    PML
    UDI-DI
    07630030862120
    PMA / PMN Number
    K241034
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    BE
    Reporter Occupation
    003

    Narratives

    Additional Manufacturer Narrative · 0

    BATCH REVIEW PERFORMED ON 17 OCT 2025. PEDICLE SCREW 03.51.10.0581 1-STEP REDUCER ENH. 2019 LOT 2161268: (B)(4) ITEMS MANUFACTURED AND RELEASED ON 22-JUN-2022. NO ANOMALIES FOUND RELATED TO THE PROBLEM. TO DATE, NO SIMILAR EVENTS HAVE BEEN REPORTED ON THE SAME LOT DURING THE PERIOD OF REVIEW. PEDICLE SCREW 03.51.10.0581 1-STEP REDUCER ENH. 2019 LOT 2155227: (B)(4) ITEMS MANUFACTURED AND RELEASED ON 24-NOV-2021 + (B)(4) ITEMS MANUFACTURED AND RELEASED ON 04-JAN-2022. NO ANOMALIES FOUND RELATED TO THE PROBLEM. TO DATE, 6 SIMILAR EVENTS HAVE BEEN REPORTED ON THE SAME LOT DURING THE PERIOD OF REVIEW. PEDICLE SCREW 03.61.324 FENESTRATED POLYAX. CANN. PED. SCR. 6X45, DUAL-DIAM (K241034) LOT 2464844: (B)(4) ITEMS MANUFACTURED AND RELEASED ON 10-DEC-2024. EXPIRATION DATE: 2029-NOV-25. NO ANOMALIES FOUND RELATED TO THE PROBLEM. TO DATE, (B)(4) ITEMS OF THE SAME LOT HAVE BEEN SOLD WITH NO SIMILAR REPORTED EVENT DURING THE PERIOD OF REVIEW. INVESTIGATION PERFORMED BY R&D PROJECT MANAGER ONE OF THE PLATES OF THE TIP THAT ACT AS INTERFACE WITH THE TULIP IS SEPARATED FROM THE INSTRUMENT DUE TO DAMAGE OF THE WELDING. THE SCREW PRESENTS DAMAGE TO THE THREAD OF THE TULIP. THIS MAY HAVE BEEN CAUSED BY NOT OPTIMAL ALIGNMENT BETWEEN THE INSTRUMENT AND THE PEDICLE SCREW HEAD, DURING REDUCTION OPERATION: IF THIS HAPPENS, THE RETAINING PINS DON'T ENTER THE RESPECTIVE SOCKET IN THE HEAD, LEADING TO EXCESSIVE LOAD ON THE WELDING. DESIGN MODIFICATIONS HAVE BEEN INTRODUCED TO WELDING INDICATIONS AND INSPECTION METHODS TO IMPROVE THE MANUFACTURING PROCESS AND POTENTIALLY REDUCE DAMAGING EVENTS. IT IS LIKELY THAT THE SUBOPTIMAL ALIGNMENT BETWEEN THE INSTRUMENT AND THE PEDICLE SCREW HEAD LED THE RETAINING PINS TO NOT ENGAGE IN THE RESPECTIVE SOCKETS IN THE SCREW HEAD, LEADING TO EXCESSIVE LOAD ON THE WELDING OF THE PLATE, IN COMBINATION WITH THE INHERENT LIMITATIONS OF THE DESIGN VERSION INVOLVED.

    Description of Event or Problem · 0

    DURING A POSTERIOR SPINAL SURGERY, THE FIRST STEP REDUCER FAILED TO PROPERLY ATTACH TO THE SCREW HEAD. INSPECTION REVEALED THAT A METAL PLATE WAS MISSING FROM THE DISTAL PART OF THE INSTRUMENT. INTRAOPERATIVE FLUOROSCOPY CONFIRMED THAT THE PIECE WAS NOT RETAINED INSIDE THE PATIENT; IT MAY HAVE ALREADY BEEN MISSING PRIOR TO SURGERY. ON THE RIGHT L5 SCREW, THE SECOND STEP REDUCER CAUSED THE SET SCREW TO REPEATEDLY CROSS-THREAD, DAMAGING THE SCREW HEAD THREADS. THIS REDUCER ALSO LOST THE SAME SMALL METAL COMPONENT. AS A RESULT, THE SURGEON REPLACED THE RIGHT L5 SCREW AND BENT THE ROD INTO GREATER LORDOSIS TO PLACE THE SET SCREW WITHOUT A PERSUADER, AS NO FUNCTIONING REDUCTION INSTRUMENT WAS AVAILABLE. SURGERY COMPLETED WITH 30/40 MIN DELAY (TOTAL TIME SURGERY 3 HOURS 10 MINUTES). NO PIECES LEFT IN THE PATIENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2249848 M.U.S.T. PEDICLE SCREW SYSTEM FENESTRATED POLYAX. CANN. PED. SCR. 6X45,DUAL-DIAM PML MEDACTA INTERNATIONAL SA 03.61.324 2464844 07630030862120

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Other