BEUDAMED
    FDA Adverse Event Injury Summary report: N

    BD SPINAL NEEDLE

    MDR report key: 1243237 · Received November 19, 2008

    Report

    Report Number
    2618282-2008-00017
    Event Type
    Injury
    Date Received
    November 19, 2008
    Manufacturer
    *
    Product Code
    BSP
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Narratives

    Additional Manufacturer Narrative · 1

    CONTACTED RPTR BY PHONE 10/24/08 TO DISCUSS PROCEDURE, OUTCOME AND ANY ADD'L SURGERY OR COMPLICATIONS. CRNA UNAVAILABLE. MESSAGE LEFT. NO RESPONSE TO DATE. CONTACTED RPTR BY LETTER ON 11/06/08. NO ADD'L INFO AVAILABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BD SPINAL NEEDLE 27G X 3 1/2 WHITACRE STERILE SPINAL NEEDLE BSP * * *

    Patients

    Seq Age Sex Outcome Treatment
    1 Other