BEUDAMED
    FDA Adverse Event Other Summary report: N

    POWERGLIDE PRO MIDLINE CATHETER

    MDR report key: 17119286 · Received June 12, 2023

    Report

    Report Number
    MW5118348
    Event Type
    Other
    Date Received
    June 12, 2023
    Report Date
    June 8, 2023
    Manufacturer
    BARD ACCESS SYSTEMS, INC.
    Product Code
    FOZ
    Report Source
    Voluntary report
    Reporter Location
    OH, US
    Reporter Occupation
    RISK MANAGER
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    GUIDEWIRE IS MISSING FROM POWERGLIDE WAND, RENDERING IT UNUSABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1308633 POWERGLIDE PRO MIDLINE CATHETER CATHETER, INTRAVASCULAR, THERAPEUTIC, SHORT-TERM LESS THAN 30 DAYS FOZ BARD ACCESS SYSTEMS, INC. F220088PT REGY0828

    Patients

    Seq Age Sex Outcome Treatment
    1 Female