BEUDAMED
    FDA Adverse Event Other Summary report: N

    RESTING PAN SPLINT

    MDR report key: 22060 · Received April 28, 1995

    Report

    Report Number
    22060
    Event Type
    Other
    Date Received
    April 28, 1995
    Date of Event
    April 24, 1995
    Report Date
    April 28, 1995
    Manufacturer
    UNKNOWN
    Product Code
    ILH
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    MN, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    UPON REMOVAL OF RESTING PAN SPLINT FROM LEFT HAND A 1 1/2 CM PRESSURE AREA/LACERATION NOTED ON BASE OF LEFT THUMB FROM EDGE OF SPLINT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RESTING PAN SPLINT RESTING PAN SPLINT ILH UNKNOWN NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 90 YR Other