BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UNK ZCA CAGE

    MDR report key: 24239718 · Received February 2, 2026

    Report

    Report Number
    0001822565-2026-00380
    Event Type
    Injury
    Date Received
    February 2, 2026
    Date of Event
    November 22, 2025
    Report Date
    February 2, 2026
    Manufacturer
    ZIMMER BIOMET, INC.
    Product Code
    JDI
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CH
    Reporter Occupation
    PHYSICIAN
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    (B)(4). D6A: IMPLANTED BETWEEN JANUARY 2007 AND JANUARY 2019. G2: FOREIGN - EVENT OCCURRED IN CHINA. G2: LITERATURE -XIAO, Q., CAO, J., XU, B., ET AL. (2025) RECONSTRUCTION OF PAPROSKY TYPE III ACETABULAR BONE DEFECTS IN REVISION HIP ARTHROPLASTY BY USING A COMBINATION OF CAGE AND MORSELIZED ALLOGRAFTS. BONE & JOINT, 6(11):1515-1522. HTTPS://DOI.ORG/10.1302/2633-1462.611.BJO-2025-0137.R1. 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 IN A JOURNAL ARTICLE THAT APPROXIMATELY FIVE YEARS POST-IMPLANTATION, ONE PATIENT UNDERWENT A HIP REVISION DUE TO CAGE MIGRATION. THE CAGE HAD MIGRATED OVER 5MM. A HEMISPHERICAL CUP AND AUGMENT WERE IMPLANTED DURING THE REVISION. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    293026 UNK ZCA CAGE PROSTHESIS, HIP JDI ZIMMER BIOMET, INC. UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Required Intervention| H