BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LAP SPONGE

    MDR report key: 33955 · Received May 20, 1996

    Report

    Report Number
    33955
    Event Type
    Injury
    Date Received
    May 20, 1996
    Date of Event
    May 7, 1996
    Report Date
    May 20, 1996
    Manufacturer
    UNKNOWN
    Product Code
    GOY
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    DE, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    RETAINED LAP SPONGE. REQUIRED REEXPLORATION OF ABDOMEN. DISCOVERED ON POST-PROCEDURE X-RAY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LAP SPONGE LAP SPONGE GOY UNKNOWN UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 62 YR Required Intervention