BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 3893292 · Received February 10, 2014

    Report

    Report Number
    3006697241-2014-00124
    Event Type
    Malfunction
    Date Received
    February 10, 2014
    Date of Event
    January 13, 2014
    Report Date
    January 13, 2014
    Manufacturer
    HILL-ROM DE MEXICO S DE RL DE CV
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CO, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND THE BRAKE CASTERS ARE OLD AND WORN AND WILL ROTATE IN A CIRCLE IF THE STRETCHER IS PUSHED FROM THE SIDE. SEE SCANNED PAGE. THE TECHNICIAN REPLACED THE BRAKE CASTERS AND BRAKE STEER CASTER TO RESOLVE THE ISSUE. BASED ON THIS INFORMATION, NO FURTHER ACTION IS REQUIRED.

    Description of Event or Problem · 1

    THE ACCOUNT REPORTED THAT THE BRAKE CASTERS WOULD ROTATE WHILE IN BRAKE MODE. THE BED WAS LOCATED ON THE THIRD FLOOR OF THE ACCOUNT. THERE IS NO PATIENT/USER INJURY REPORTED. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT # (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    88818 TRANSTAR STRETCHER A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM DE MEXICO S DE RL DE CV 8000

    Patients

    Seq Age Sex Outcome Treatment
    1