BEUDAMED
    FDA Adverse Event Other Summary report: N

    MILTEX

    MDR report key: 137747 · Received January 14, 1997

    Report

    Report Number
    2431021-1997-90003
    Event Type
    Other
    Date Received
    January 14, 1997
    Manufacturer
    MILTEX INSTRUMENT CO.
    Product Code
    FMF
    Report Source
    Manufacturer report
    Reporter Location
    CA
    Reporter Occupation
    DENTIST

    Narratives

    Description of Event or Problem · 1

    AFTER DR INJECTED PT WITH A MANDIBULAR BLOC, HE REMOVED SYRINGE FROM PT'S MOUTH, WENT TO REMOVE THE NEEDLE FROM THE SYRINGE, FOUND NEEDLE NOT PRESENT IN THE SYRINGE, LOOKED IMMEDIATELY IN PT'S MOUTH, FOUND NEEDLE WITH "HUB" ATTACHED, REMOVED IT SUCCESSFULLY WITHOUT INCIDENT. NO PT INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MILTEX SELF ASPIRATING SYRINGE FMF MILTEX INSTRUMENT CO. SELF ASPIRATING SYRINGE UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 * Required Intervention