BEUDAMED
    FDA Adverse Event Other Summary report: N

    VERSACUT

    MDR report key: 3015747 · Received March 14, 2013

    Report

    Report Number
    MW5029424
    Event Type
    Other
    Date Received
    March 14, 2013
    Report Date
    March 14, 2013
    Manufacturer
    LUMENIS
    Product Code
    GCJ
    Report Source
    Voluntary report
    Reporter Location
    GA, US
    Reporter Occupation
    BIOMEDICAL ENGINEER

    Narratives

    Description of Event or Problem · 1

    ADDRESSING PRODUCT RECALL. LUMENIS LIMITED. VERSACUT MORCELLATOR. WE DO NOT HAVE THIS ITEM IN OUR INVENTORY. NO FURTHER ACTION NEEDED AT OUR FACILITY. THANKS, BIOMED DEPT., (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    108526 VERSACUT MORCELLATOR GCJ LUMENIS ALL

    Patients

    Seq Age Sex Outcome Treatment
    1