BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BAXTER

    MDR report key: 366068 · Received December 12, 2001

    Report

    Report Number
    MW1023592
    Event Type
    Malfunction
    Date Received
    December 12, 2001
    Date of Event
    October 10, 2001
    Report Date
    October 10, 2001
    Manufacturer
    MEDIQ PRN
    Product Code
    FRN
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    RPTR HAS NOTICED THAT MANY OF THE INFUSION PUMPS IN THE HOSP HAVE NOT BEEN SERVICED REGULARLY BY THE HOSP'S RENTAL CO. THIS IS NOT RIGHT. THEY NEED TO BE INSPECTED AND TESTED PER MFR SPECS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    56168 BAXTER INFUSION DEVICES FRN MEDIQ PRN * *

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other