BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    READYMED

    MDR report key: 14724 · Received July 15, 1994

    Report

    Report Number
    MW1002845
    Event Type
    Malfunction
    Date Received
    July 15, 1994
    Date of Event
    May 30, 1994
    Report Date
    July 6, 1994
    Manufacturer
    MCGAW, INC.
    Product Code
    MEB
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    VA, US
    Reporter Occupation
    PHARMACIST

    Narratives

    Description of Event or Problem · 1

    PT REPORTED PUMP NOT INFUSING, LPN FOUND PUMP TO NOT OWRK. LPN TOOK PUMP AND INADVERTENTLY DISPOSED OF IT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 READYMED ELASTOMERIC INFUSION DEVICE MEB MCGAW, INC. 94C012

    Patients

    Seq Age Sex Outcome Treatment
    1 74 YR Other