BEUDAMED
    FDA Adverse Event Other Summary report: N

    NEURO-TRACE NEEDLE

    MDR report key: 571419 · Received February 9, 2005

    Report

    Report Number
    2925153-2005-00023
    Event Type
    Other
    Date Received
    February 9, 2005
    Report Date
    February 8, 2005
    Manufacturer
    HDC CORP.
    Product Code
    HAS
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MO, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    "NEEDLES WERE BLOCKED WHEN MEDICATION WAS INSERTED. DOCTOR TRIED TO RE-START THE PROCEDURE AND NEEDLES WERE BLOCKED. NO INJURY REPORTED OR MEDICAL INTERVENTION WAS NEEDED."

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NEURO-TRACE NEEDLE NEURO-TRACE NEEDLE HAS HDC CORP. 556-23-04 0106

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other