BEUDAMED
    FDA Adverse Event Injury Summary report: N

    REFLECTION

    MDR report key: 2511298 · Received March 30, 2012

    Report

    Report Number
    1020279-2012-00200
    Event Type
    Injury
    Date Received
    March 30, 2012
    Date of Event
    March 10, 2012
    Report Date
    March 10, 2012
    Manufacturer
    SMITH & NEPHEW, INC
    Product Code
    JDH
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    HI, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED SURGERY WAS DELAYED DUE THE DEVICE NOT LOCKING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 REFLECTION LINER ADAPTOR JDH SMITH & NEPHEW, INC 04EM17169

    Patients

    Seq Age Sex Outcome Treatment
    1 Hospitalization