BEUDAMED
    FDA Adverse Event Death Summary report: N

    ZIMMER

    MDR report key: 49801 · Received November 11, 1996

    Report

    Report Number
    1822565-1996-00632
    Event Type
    Death
    Date Received
    November 11, 1996
    Report Date
    November 8, 1996
    Manufacturer
    ZIMMER, INC.
    Product Code
    LOD
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    PT EXPIRED FOLLOWING THE IMPLANT OF A CEMENTED PROSTHESIS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ZIMMER Implant OSTEOBOND BONE CEMENT LOD ZIMMER, INC. NA 71652400

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Death