BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MPL HYPO

    MDR report key: 211874 · Received February 26, 1999

    Report

    Report Number
    1412902-1999-00003
    Event Type
    Injury
    Date Received
    February 26, 1999
    Date of Event
    January 8, 1999
    Report Date
    January 22, 1999
    Manufacturer
    MPL TECHNOLOGIES
    Product Code
    DZM
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SW
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    ORAL SURGERY WAS NEEDED TO REMOVE A DENTAL NEEDLE FRAGMENT FROM A PT'S CHEEK.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MPL HYPO DENTAL NEEDLE DZM MPL TECHNOLOGIES 30G SHORT UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Required Intervention