BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 3812568 · Received April 17, 2014

    Report

    Report Number
    3006697241-2014-00366
    Event Type
    Malfunction
    Date Received
    April 17, 2014
    Date of Event
    March 22, 2014
    Report Date
    March 22, 2014
    Manufacturer
    HILLROM DE MEXICO S DE RL DE CV
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND ALL 4 BRAKE CASTERS NOT HOLDING AND A BROKEN SCREW IN THE HEX ROD. A SEARCH OF THE HILL-ROM MAINTENANCE RECORDS SHOWED HILL-ROM PERFORMED PREVENTATIVE MAINTENANCE ON THIS BED IN 2007 AND 2008-2013. IT IS UNKNOWN IF THE FACILITY PERFORMED ANY OTHER PREVENTATIVE MAINTENANCE ON THIS BED. THE TECHNICIAN REPLACED ALL 4 CASTERS AND THE HEX ROD TO RESOLVE THE ISSUE. BASED ON THIS INFORMATION, NO FURTHER ACTION IS REQUIRED.

    Description of Event or Problem · 1

    HILL-ROM RECEIVED A REPORT FROM A HILL-ROM TECHNICIAN STATING THE STRETCHER STILL ROLLS AFTER BRAKE/STEER PEDAL HAS BEEN PUT INTO THE BRAKE POSITION. THE BED WAS LOCATED AT THE ACCOUNT IN ER. THERE WAS NO PATIENT/USER INJURY REPORTED. THIS REPORTED WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    236019 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILLROM DE MEXICO S DE RL DE CV 8050

    Patients

    Seq Age Sex Outcome Treatment
    1