BEUDAMED
    FDA Adverse Event Injury Summary report: N

    G7 OSSEOTI MULTIHOLE 58MM G

    MDR report key: 25230202 · Received May 20, 2026

    Report

    Report Number
    0001825034-2026-01353
    Event Type
    Injury
    Date Received
    May 20, 2026
    Date of Event
    April 30, 2026
    Report Date
    May 20, 2026
    Manufacturer
    ZIMMER BIOMET, INC.
    Product Code
    LPH
    PMA / PMN Number
    K140669
    Removal / Correction Number
    N/A
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AS
    Reporter Occupation
    PHYSICIAN
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    (B)(4). H10: ARCOS 15X150 MM SPL TPR DIST, ITEM: 11-300815, LOT: 65750703. ARCOS CON SZ C STD 60 MM, ITEM: 11-301303, LOT: 65710916. G7 HI-WALL E1 LINER 36 MM G, ITEM: 010000937, LOT: 7210981. G7 SCREW 6.5 MM X 30 MM, ITEM: 010000999, LOT: 7389732. DELTA CERAMIC FEM HD 36/-3 MM, ITEM: 650-0660, LOT: 3095592. G2: FOREIGN ¿ AUSTRALIA. THE PRODUCT WAS REQUESTED BUT WAS NOT RETURNED BY THE HOSPITAL AND WILL THEREFORE NOT BE SENT TO ZIMMER BIOMET FOR INVESTIGATION. ONCE THE INVESTIGATION HAS BEEN COMPLETED, A SUPPLEMENTAL MDR WILL BE SUBMITTED.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT THE PATIENT UNDERWENT A HIP REVISION APPROXIMATELY THREE YEARS POST-IMPLANTATION DUE TO PAIN AND RADIOLUCENCY OF COMPONENT. IT WAS CONFIRMED THAT NO FURTHER INFORMATION COULD BE PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    393203 G7 OSSEOTI MULTIHOLE 58MM G PROSTHESIS, HIP LPH ZIMMER BIOMET, INC. 7196540

    Patients

    Seq Age Sex Outcome Treatment
    1