BEUDAMED
    FDA Adverse Event Death Summary report: N

    BIOMET HIP SYSTEM

    MDR report key: 24662070 · Received March 23, 2026

    Report

    Report Number
    0001825034-2026-00680
    Event Type
    Death
    Date Received
    March 23, 2026
    Date of Event
    July 13, 2022
    Report Date
    March 23, 2026
    Manufacturer
    ZIMMER BIOMET, INC.
    Product Code
    LPH
    PMA / PMN Number
    K990830
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NL
    Reporter Occupation
    PHYSICIAN
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    (B)(4). D10: CAT# 650-0325 LOT# 7183169 TPRLOC COCR CMTD STEM T1 7.5MM. G2: FOREIGN ¿ EVENT OCCURRED IN THE NETHERLANDS. H6: PROPOSED COMPONENT CODE: MECHANICAL (G04) - HEAD. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS; HOWEVER, AN INVESTIGATION OF THE REPORTED EVENT IS IN PROGRESS. ONCE THE INVESTIGATION IS COMPLETED, A SUPPLEMENTAL MEDWATCH 3500A WILL BE SUBMITTED.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT APPROXIMATELY THREE WEEKS POST RIGHT HIP IMPLANTATION, THE PATIENT PASSED AWAY. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    720762 BIOMET HIP SYSTEM PROSTHESIS, HIP LPH ZIMMER BIOMET, INC. 64850323

    Patients

    Seq Age Sex Outcome Treatment
    1 85 YR Female Death