BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 3130284 · Received February 25, 2013

    Report

    Report Number
    3006697241-2013-00041
    Event Type
    Malfunction
    Date Received
    February 25, 2013
    Manufacturer
    HILL-ROM DE MEXICO S DE RL DE CV
    Product Code
    FPO
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNT IS NOT GOING TO REPAIR THE STRETCHER AT THIS TIME.

    Description of Event or Problem · 1

    REFERENCE IMPORTER REPORT NUMBER (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    81156 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM DE MEXICO S DE RL DE CV

    Patients

    Seq Age Sex Outcome Treatment
    1