BEUDAMED
    FDA Adverse Event Summary report: N

    ZIMMER BIOMET COMPANY

    MDR report key: 16113228 · Received January 5, 2023

    Report

    Report Number
    MW5114203
    Date Received
    January 5, 2023
    Date of Event
    December 12, 2022
    Report Date
    December 23, 2022
    Manufacturer
    ZIMMER BIOMET G. K.
    Product Code
    JDI
    Report Source
    Voluntary report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    PT RECEIVING TOTAL HIP ARTHROPLASTY. THE GUIDE ROD BROKE AND THE TIP SNAPPED OFF. C-ARM TO CONFIRM NOT IN PT (B)(6) 2022. "G.7 GUIDE ROD BROKE DURING SURGERY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    438978 ZIMMER BIOMET COMPANY PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, CEMENTED JDI ZIMMER BIOMET G. K.

    Patients

    Seq Age Sex Outcome Treatment
    1 64 YR Female