BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MUSTMINI OCCIPITAL SCREW

    MDR report key: 21353184 · Received February 11, 2025

    Report

    Report Number
    3005180920-2025-00073
    Event Type
    Injury
    Date Received
    February 11, 2025
    Date of Event
    January 16, 2025
    Report Date
    May 2, 2025
    Manufacturer
    MEDACTA INTERNATIONAL SA
    Product Code
    NKG
    UDI-DI
    07630030865398
    PMA / PMN Number
    K182837
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    BE
    Reporter Occupation
    003

    Narratives

    Additional Manufacturer Narrative · 0

    FOLLOW UP 1: - PIECE RETURNED ON 24 APRIL 2025. - VISUAL INSPECTION. - DEVICES DETAILS. - REVISION SURGERY YEAR. - EVENT DESCRIPTION UPDATED (B5). - CODES UPDATE AND CORRECTIONS (H6). BATCH REVIEW PERFORMED ON 14 APRIL 2025 LOT 2459956: (B)(4) ITEMS MANUFACTURED AND RELEASED ON 01-JUL-2024. EXPIRATION DATE: 2029-06-05. NO ANOMALIES FOUND RELATED TO THE PROBLEM. TO DATE, (B)(4) ITEMS OF THE SAME LOT HAVE BEEN SOLD WITH ONE SIMILAR REPORTED EVENT DURING THE PERIOD OF REVIEW. ADDITIONAL ITEM INVOLVED IN THE EVENT, BATCH REVIEW PERFORMED ON 14 APRIL 2025: MUST MINI 03.75.802 MUST MINI OCCIPITAL SCREW, Ø4 X 8MM (STE) (K182837) LOT. 2458996. LOT 2458996: (B)(4) ITEMS MANUFACTURED AND RELEASED ON 27-MAY-2024. EXPIRATION DATE: 2029-04-24. NO ANOMALIES FOUND RELATED TO THE PROBLEM. TO DATE, (B)(4) ITEMS OF THE SAME LOT HAVE BEEN SOLD WITH ONE SIMILAR REPORTED EVENT DURING THE PERIOD OF REVIEW. MUST MINI 03.75.800 MUST MINI OCCIPITAL SCREW, Ø4 X 6MM (STE) (K182837) LOT. 2459827 LOT 2459827: (B)(4) ITEMS MANUFACTURED AND RELEASED ON 12-JUL-2024. EXPIRATION DATE: 2029-05-16. 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. MUST MINI 03.75.801 MUST MINI OCCIPITAL SCREW, Ø4 X 7MM (STE) (K182837) LOT. 1921826 LOT 1921826: (B)(4) ITEMS MANUFACTURED AND RELEASED ON 03-JUN-2019. EXPIRATION DATE: 2024-05-19. 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. (2 DEVICES INVOLVED IN THIS COMPLAINT). VISUAL INSPECTION PERFORMED BY R&D MANAGER BASED ON THE VISUAL INSPECTION PERFORMED ON THE RETRIEVED DEVICES, NO VISUAL DEFECTS AND/OR ANOMALIES WERE OBSERVED. BOTH THE SCREWS AND PLATE DEVICE WERE INTACT AND EXPECTED TO BE FUNCTIONAL AS A VIRGIN ONES. ADDITIONAL CONSIDERATION AS FOLLOWING: 1) THE PLATE WAS STRAIGHT, AND NOT CONTOURED DURING THE SURGERY. THE PLATE CAN BE CONTOURED TO IMPROVE THE CONTACT SURFACE WITH THE BONE BASED ON INDIVIDUAL ANATOMY, REDUCING THE CLEARANCE BETWEEN THE DEVICE AND THE BONE AS WELL AS IMPROVING THE SCREW BONE PURCHASE. THE CONTOURING OF THE PLATE MAKES IT FLUSH TO THE BONE AS WELL AS IMPROVE THE BONE PURCHASE OF SCREWS, IN PARTICULAR IN THINNER CORTICAL BONE. 2) THE POST X-RAY WERE NOT AVAILABLE AND IT WAS NOT POSSIBLE TO VERIFY THE FINAL POSITION OF THE PLATE AND THE EFFECTIVE BONE PURCHASE OF THE SCREWS. 3) IT IS NOT CLEAR IF THE SCREW HOLE PREPARATION WAS CORRECTLY PERFORMED TO CREATE THE PATH FOR THE SCREWS BASED ON THE IDENTIFIED DIAMETER AND LENGTH. THIS SOLUTION HELPS THE POSITIONING OF SCREWS, IN PARTICULAR WHEN THE BONE IS SCLEROTIC AND THE RISK OF STRIP-OFF THE BONE IS HIGHER. 4) OC SCREWS FIXATION FORCE IS DEFINED UNDER DISCREPTION OF USERS AND REMAIN UNKNOWN. IT IS SUPPOSED THAT UNSUFFICIENT FIXATION AND A POSSIBLE CLEARANCE BETWEEN THE PLATE AND THE BONE MAY LEAD TO MICROMOTION OF THE PLATE WITH INCREASED RISK FOR SCREWS LOOSENING. 5) THE INDIVIDUAL CONDITION OF THE BONE, OSTEOPOROTIC VS SCLEROTIC, AND THE THICKNESS OF THE CORTICAL BONE CAN AFFECT THE SUCCESS/UNSUCCESS OF THE SURGERY, IN TERMS OF OPTIMAL BONE PURCHASE AND FINAL STABILITY. IN CONCLUSION ,CONSIDERING ALL THE POSSIBLE VARIATION ANALYSED WITHIN THIS CASE IT WAS NOT POSSIBLE TO DEFINE THE REAL ROOT CAUSE THAT LED TO SCREWS LOOSENING AND SUBSEQUENT SURGERY FAILURE. ROOT CAUSE: BASED ON THE INFORMATION AVAILABLE, NO DEFINITIVE ROOT CAUSE CAN BE ESTABLISHED, WHILE THE DEVICE HISTORY RECORD REVIEW DOES NOT INDICATE ANY POTENTIAL MANUFACTURING-RELATED ISSUE. ALTHOUGH IT CANNOT BE CONFIRMED, THE ISSUE REPORTED MAY HAVE RESULTED FROM APPLICATION-SPECIFIC FACTORS AND/OR PATIENT-RELATED CONDITIONS, SUCH AS LIMITED BONE QUALITY, IN COMBINATION WITH POTENTIAL INTRAOPERATIVE VARIABLES, INCLUDING PLATE CONTOURING, SCREW HOLE PREPARATION, AND SCREW FIXATION ANOMALIES.

    Description of Event or Problem · 0

    THE OCCIPITAL SCREWS FROM THE OCCIPITAL PLATE CAME LOOSE. PRIMARY SURGERY WAS PERFORMED ON (B)(6) 2024. REVISION SURGERY WILL BE PERFORMED SOON.

    Description of Event or Problem · 0

    THE OCCIPITAL SCREWS FROM THE OCCIPITAL PLATE CAME LOOSE. PRIMARY SURGERY WAS PERFORMED ON (B)(6) 2024. REVISION SURGERY PERFORMED IN 2025 (EXACT DATE UNKNOWN).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1754177 MUSTMINI OCCIPITAL SCREW MUST MINI OCCIPITAL SCREW, Ø4 X 6MM NKG MEDACTA INTERNATIONAL SA 03.75.800 2459956 07630030865398

    Patients

    Seq Age Sex Outcome Treatment
    1 78 YR Female Required Intervention