BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MEDFUSION 2001H SYRINGE INFUSION PUMP

    MDR report key: 311397 · Received January 5, 2001

    Report

    Report Number
    1036813-2001-00002
    Event Type
    Malfunction
    Date Received
    January 5, 2001
    Date of Event
    December 6, 2000
    Report Date
    December 6, 2000
    Manufacturer
    MEDEX
    Product Code
    FRN
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    DURING IN-HOUSE EVAL, THE UNIT ACCEPTED A 60CC BD SYRINGE AS A 30CC SYRINGE. NO PT INJURY OR TREATMENT WAS ASSOCIATED WITH THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    532 MEDFUSION 2001H SYRINGE INFUSION PUMP SYRINGE INFUSION PUMP FRN MEDEX 2001H NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN