BEUDAMED
    FDA Adverse Event Injury Summary report: N

    DELTA SPLINT LONGUETTE

    MDR report key: 477641 · Received August 13, 2003

    Report

    Report Number
    1818910-2003-00514
    Event Type
    Injury
    Date Received
    August 13, 2003
    Date of Event
    July 15, 2003
    Report Date
    July 15, 2003
    Manufacturer
    DEPUY-NORTH BRUNSWICK CASTING PRODUCTS DIV.
    Product Code
    FYH
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GM
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    PT GOT MACERATION IN THEIR INNER HAND AFTER A DELTA SPLINT LONGUETTE WAS APPLIED DUE TO A MIDDLE-BONE FRACTURE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DELTA SPLINT LONGUETTE CASTING PRODUCT FYH DEPUY-NORTH BRUNSWICK CASTING PRODUCTS DIV. NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Required Intervention