BEUDAMED
    FDA Adverse Event Injury Summary report: N

    1020279-2011-00086

    MDR report key: 2022738 · Received March 17, 2011

    Report

    Report Number
    1020279-2011-00086
    Event Type
    Injury
    Date Received
    March 17, 2011
    Report Date
    March 17, 2011
    Manufacturer
    SMITH & NEPHEW ORTHOPAEDICS
    Product Code
    HSD
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TN, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    LEGAL CLAIMANT PROPOSES NEGLIGENCE OF MEDICAL CARE OR TREATMENT. THE TYPE OF S&N IMPLANT INVOLVED IS UNKNOWN AT THIS TIME.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HSD SMITH & NEPHEW ORTHOPAEDICS

    Patients

    Seq Age Sex Outcome Treatment
    1