BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SULZER MEDICA

    MDR report key: 330181 · Received April 23, 2001

    Report

    Report Number
    330181
    Event Type
    Malfunction
    Date Received
    April 23, 2001
    Date of Event
    June 5, 2000
    Report Date
    March 19, 2001
    Manufacturer
    SULZER MEDICA
    Product Code
    LPH
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    PRODUCT RECALL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    18601 SULZER MEDICA FEMORAL HEAD ACETABULAR SHELL ACETABULAR LINER LPH SULZER MEDICA 1417767 1412460

    Patients

    Seq Age Sex Outcome Treatment
    1 49 YR Other