BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SULZERMEDICA

    MDR report key: 331139 · Received May 3, 2001

    Report

    Report Number
    MW1021800
    Event Type
    Injury
    Date Received
    May 3, 2001
    Date of Event
    June 5, 2000
    Report Date
    May 3, 2001
    Manufacturer
    SULZER MEDICA, SULZER ORTHOPEDICS, INC.
    Product Code
    LPH
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    LA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    PT HAS BEEN EXPERIENCING PROBLEMS S/P SULZER TOTAL HIP REPLACEMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    20291 SULZERMEDICA INTER-OP ACETABULAR SYSTEM HEMISPHERICAL POROUS SHELL LPH SULZER MEDICA, SULZER ORTHOPEDICS, INC. * 1421771

    Patients

    Seq Age Sex Outcome Treatment
    1 43 YR Disability