BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BD 22 IV CATHETER

    MDR report key: 22511055 · Received July 15, 2025

    Report

    Report Number
    MW5172697
    Event Type
    Malfunction
    Date Received
    July 15, 2025
    Date of Event
    July 8, 2025
    Report Date
    July 11, 2025
    Manufacturer
    BECTON DICKINSON AND COMPANY
    Product Code
    FOZ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    SC, US
    Reporter Occupation
    RISK MANAGER
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    LOT #5043113 ## 22 IV CATHETER NEEDLE RETRACTED PREMATURELY AND WITHOUT PRESSING BUTTON WHILE INSERTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    544062 BD 22 IV CATHETER CATHETER, INTRAVASCULAR, THERAPEUTIC, SHORT-TERM LESS THAN 30 DAYS FOZ BECTON DICKINSON AND COMPANY 5043113

    Patients

    Seq Age Sex Outcome Treatment
    1 82 YR Female Other