BEUDAMED
    FDA Adverse Event Injury Summary report: N

    BD ULTRA-FINE 3/10CC INSULIN SYRINGE

    MDR report key: 266614 · Received March 1, 2000

    Report

    Report Number
    1920898-2000-00003
    Event Type
    Injury
    Date Received
    March 1, 2000
    Report Date
    February 28, 2000
    Manufacturer
    BECTON DICKINSON
    Product Code
    FMF
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    SURGERY REQUIRED ON 01/14/2000 TO REMOVE NEEDLE FROM LEFT THIGH.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BD ULTRA-FINE 3/10CC INSULIN SYRINGE SYRINGE FMF BECTON DICKINSON NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Required Intervention