BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSPORT STRETCHER

    MDR report key: 2243475 · Received August 11, 2011

    Report

    Report Number
    3006697241-2011-00079
    Event Type
    Malfunction
    Date Received
    August 11, 2011
    Date of Event
    August 1, 2011
    Report Date
    August 1, 2011
    Manufacturer
    HILL-ROM DE MEXICO S DE RL DE CV
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNT REPLACED THE SHOULDER BOLT TO REPAIR THE STRETCHER.

    Description of Event or Problem · 1

    INFO RECEIVED INDICATES THE LEFT SIDERAIL WILL NOT LATCH DUE TO THE LATCH ASSEMBLY SHOULDER BOLT BACKING OUT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRANSPORT STRETCHER WHEELED STRETCHER FPO HILL-ROM DE MEXICO S DE RL DE CV 8005

    Patients

    Seq Age Sex Outcome Treatment
    1