BEUDAMED
    FDA Adverse Event Injury Summary report: N

    BD 33G LANCET

    MDR report key: 3802861 · Received May 1, 2014

    Report

    Report Number
    2243072-2014-00092
    Event Type
    Injury
    Date Received
    May 1, 2014
    Report Date
    April 29, 2014
    Manufacturer
    BD
    Product Code
    FMK
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    JA
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    THE SAMPLE IS AVAILABLE FOR EVALUATION. UPON COMPLETION OF THE INVESTIGATION, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. (B)(4).

    Description of Event or Problem · 1

    THE PHYSICIAN DETECTED A LUMP ON THE PATIENT'S MIDDLE FINGER. THE PHYSICIAN CUT THE FINGER OPEN TO FIND OUT WHAT IT WAS AND FOUND A NEEDLE INSIDE. THE NEEDLE WAS REMOVED SUCCESSFULLY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    261163 BD 33G LANCET 33G LANCET FMK BD UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK Required Intervention