BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ZIMMER

    MDR report key: 51702 · Received September 24, 1996

    Report

    Report Number
    1822565-1996-00603
    Event Type
    Malfunction
    Date Received
    September 24, 1996
    Report Date
    September 24, 1996
    Manufacturer
    ZIMMER, INC.
    Product Code
    HXZ
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    JAW OF DEVICE FRACTURED. NO PATIENT INVOLVEMENT REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ZIMMER PIN CUTTER HXZ ZIMMER, INC. NA 58761500

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN