BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ZIMMER

    MDR report key: 756435 · Received August 15, 2006

    Report

    Report Number
    MW1040191
    Event Type
    Injury
    Date Received
    August 15, 2006
    Manufacturer
    *
    Product Code
    LXH
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    ZIMMER COUS PART #93-76-00-000, CE0123, 2808-6103313. THIS ITEM WAS TAKEN FROM AN INSTRUMENT SET. THIS PART IS USED IN ORTHOPEDIC SURGERY AND IS IMPOSSIBLE TO THOROUGHLY CLEAN. THIS PART SHOULD BE ABLE TO BE DISASSEMBLED, HOWEVER IT IS NOT. IT IS A PT SAFETY ISSUE WHEN THE SURGICAL INSTRUMENT CANNOT BE THOROUGHLY CLEANED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ZIMMER ORTHO INSTRUMENT LXH * 9376-00-000 *

    Patients

    Seq Age Sex Outcome Treatment
    1 *