BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UNK

    MDR report key: 502736 · Received December 19, 2003

    Report

    Report Number
    502736
    Event Type
    Injury
    Date Received
    December 19, 2003
    Date of Event
    April 11, 2003
    Report Date
    December 18, 2003
    Manufacturer
    NA
    Product Code
    HRX
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    PA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    IN 2003, THE PATIENT HAD A CARPAL TUNNEL RELEASE, PERFORMED ON THE LEFT HAND. ONE WK LATER, THE PATIENT RETURNED TO THE OPERATING ROOM FOR AN EXPLORATION OF THE LEFT MEDIAN NERVE, SECONDARY TO NUMBNESS. THE SENSORY PORTION OF THE LEFT MEDIAN NERVE WAS FOUND TO BE LACERATED. A REPAIR OF THE LEFT MEDIAN NERVE WAS PERFORMED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 UNK UNK HRX NA UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 56 YR Required Intervention