BEUDAMED
    FDA Adverse Event Injury Summary report: N

    INBONE DRIVE TIBIA REAMER

    MDR report key: 24372785 · Received February 17, 2026

    Report

    Report Number
    3010667733-2026-00132
    Event Type
    Injury
    Date Received
    February 17, 2026
    Date of Event
    January 23, 2026
    Report Date
    May 6, 2026
    Manufacturer
    WRIGHT MEDICAL TECHNOLOGY INC
    Product Code
    HTO
    UDI-DI
    00840420196187
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IA, US
    Reporter Occupation
    OTHER
    Health Professional
    N

    Narratives

    Additional Manufacturer Narrative · 0

    ADDITIONAL INFORMATION HAS BEEN REQUESTED AND IF RECEIVED, WILL BE PROVIDED IN THE SUPPLEMENTAL REPORT.

    Description of Event or Problem · 0

    AS REPORTED: "THE PRODUCT WAS THROWN AWAY IN THE TRASH BECAUSE THE REAMER HEAD PIECE 14MM (B)(6) WAS BROKEN OFF ON THE REAMER ROD (200089). THE WRENCH SLID A LITTLE BIT AND BROKE THE MEDIAL MAL OR DISTAL TIBIA AND WE HAD TO FIX THE DISTAL TIBIA WITH ORIF WITH A MEDIAL MAL PLATE".

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    499698 INBONE DRIVE TIBIA REAMER REAMER HTO WRIGHT MEDICAL TECHNOLOGY INC UNKNOWN 00840420196187

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Required Intervention