BEUDAMED
    FDA Adverse Event Other Summary report: N

    BARD

    MDR report key: 805564 · Received December 29, 2006

    Report

    Report Number
    805564
    Event Type
    Other
    Date Received
    December 29, 2006
    Date of Event
    November 16, 2006
    Report Date
    November 17, 2006
    Manufacturer
    CR BARD
    Product Code
    FCG
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    FL, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    DURING PROCEDURE, NEEDLE BROKE OFF IN PT AT THE HUB REQUIRING MANUAL EXTRACTION OF NEEDLE FROM THE PT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BARD OSTYCUT BONE BIOPSY NEEDLE FCG CR BARD UNK ANQC0750

    Patients

    Seq Age Sex Outcome Treatment
    1 59 YR Other