BEUDAMED
    FDA Adverse Event Other Summary report: N

    VENI-GRAD TM

    MDR report key: 376602 · Received February 14, 2002

    Report

    Report Number
    1317214-2002-00004
    Event Type
    Other
    Date Received
    February 14, 2002
    Date of Event
    December 6, 2001
    Report Date
    January 14, 2002
    Manufacturer
    CONMED CORPORATION
    Product Code
    KMK
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MO, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT, "AN ELDERLY PT SUFFERED A SKIN TEAR WHEN THE VENI-GARD (IV STABILIZATION DEVICE) WAS REMOVED. A SKIN & WOUND CARE SPECIALIST WAS CALLED IN TO EVALUATE THE REPORTED INJURY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VENI-GRAD TM I.V. STABILIZATION DRESSING KMK CONMED CORPORATION NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other