BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    OBGYN TRANSTAR

    MDR report key: 2132438 · Received June 14, 2011

    Report

    Report Number
    1824206-2011-03251
    Event Type
    Malfunction
    Date Received
    June 14, 2011
    Date of Event
    June 2, 2011
    Report Date
    June 2, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECH FOUND THE LEFT SIDERAIL WAS NOT LATCHING AS THE SCREW FOR THE LATCH WAS MISSING. REPLACED SHOULDER SCREW TO RESOLVE THIS ISSUE. BED FOUND OUTSIDE ED.

    Description of Event or Problem · 1

    COMPLAINT RECEIVED THAT THE LEFT SIDERAIL WAS NOT LATCHING. NO PT IMPACT. BED LOCATED OUTSIDE ED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 OBGYN TRANSTAR WHEELED STRETCHER FPO HILL-ROM, INC. P8050

    Patients

    Seq Age Sex Outcome Treatment
    1